Heart Arrest, Out-Of-Hospital
Conditions
Brief summary
Phase II double blind (participants and investigator) placebo controlled randomized (1:1) clinical trial of inhaled nitric oxide (iNO) 20 ppm administered over 12h beginning as soon as possible but within 4 h of return of spontaneous circulation (ROSC) from out-of-hospital cardiac arrest (OHCA). Planned enrollment is 180 subjects over 48 months at University of Pittsburgh Medical Center (UPMC) Hospitals with randomization stratified in blocks of 8. Recruitment will be performed under exception from informed consent (EFIC) to facilitate early enrollment and treatment. The study will have a pre-specified safety analysis at the mid-point (after 1 year or 60 patients whichever occurs first). Subjects will be screened by members of the University of Pittsburgh post-cardiac arrest service (PCAS), all of whom will serve as the study co-investigators, and the Research Coordinators. Notification of inclusion under EFIC will be performed as soon as possible by a member of the study team generally to a surrogate as the subjects will be comatose after OHCA.
Detailed description
Subjects will be identified upon emergency department (ED) arrival or upon transfer from an outside facility and screened for enrollment by a PCAS physician as soon as possible. Eligible patients will have receive any required resuscitation (including central venous and arterial line placement, endotracheal intubation and hemodynamic resuscitation as needed) prior to having baseline labs and studies performed. Subjects will then be started on study drug delivered via the mechanical ventilator with a concealed canister (subject, providers and outcome assessors blind to treatment assignment). Randomization will be performed 1:1 in blocks of 8 using a random number generator. A randomization list will be prepared in advance by the director of respiratory therapy (RT) at each site and verified by a company representative. These individuals (who are not part of the study team) will be unblinded and assure that allocation to placebo and intervention is accurate. The allocation list will assign study drug canisters (by barcode) to each subject in order of study ID. Treatment assignment will be revealed after opening a sealed opaque envelope once enrollment is confirmed by a physician investigator. Study drug will then be administered by RT based on allocation. During study drug administration hourly vital signs will be obtained and methemoglobin levels for safety. Study drug will be weaned off after 12h over the course of 1h (10, 5, 4, 3, 2, 1 ppm each for 10 min) prior to discontinuation. Subjects will then receive standard post-resuscitation care with outcomes assessed by a blinded study team member (see below for outcomes). Additional clinical variables to be collected Demographics and baseline function. Age, sex, race, maximum education level, employment status, marital status, Barthel activities of daily living (ADL) index prior to OHCA. Arrest data. Location of OHCA, witnessed, bystander cardiopulmonary resuscitation (CPR), estimated no flow and low flow times, presenting rhythm, doses of epinephrine administered, shocks administered, recurrent arrest, date and time of ROSC. Medical comorbidities. Diabetes, hypertension, active smoking, hyperlipidemia, chronic obstructive pulmonary disease (COPD), hypertension, drug abuse, prior myocardial infarction, prior coronary artery bypass grafting (CABG), prior coronary angiography with angioplasty or stent, congestive heart failure (EF on last echocardiogram \[ECHO\] prior to OHCA), obstructive sleep apnea, pulmonary hypertension, calculated Charlson comorbidity index (CCI). Home medications. Statins, nitrates, anticoagulation, antiplatelet agents Hospital Interventions. Coronary angiography, percutaneous coronary intervention, CABG, mechanical ventilation hours and fraction of inspired oxygen (FiO2) from 0-24h after therapy start In-hospital medications. Alteplase, anti-epileptic medication use (valproate, phenytoin, lacosamide, levetiracetam), neurostimulants (methylphenidate, bromocriptine, modafinil, amantadine), cumulative dose of fentanyl, propofol, midazolam, cis-atracurium and vecuronium in at 24 (+/- 12 hours), 48 (+/- 12 hours), and 72 (+/- 12 hours) hours after therapy initiation Data Storage Subjects will be assigned a study identifier (ID) upon entry and all data/samples stored using that ID. Linkage to patient identifiers will be maintained in a secure spreadsheet and will include name, date of birth and medical record number. Clinical data will be entered on case report forms (source documentation) which will be stored in a locked filing cabinet within a locked office assigned to the study team. Deidentified clinical and lab data will all be subsequently entered from the case report forms into a web based database (REDCap) to be maintained by Dr. Dezfulian's research assistant who has prior experience from other studies. Statistical Analysis Plan Continuous data will be compared using t-tests and repeated measures ANOVA to compare between iNO and placebo groups at multiple times. Dichotomous outcomes including the primary endpoint will be compared by chi squared test. Time to awakening and 90d survival will be compared by log rank test of Kaplan-Meier survival plots. All tests will be two tailed with unadjusted p\<0.05 considered significant. In the event of a differential distribution of baseline variables strongly associated with outcome (univariate OR \>2), dichotomous outcomes will be adjusted for these baseline variables.
Interventions
DRUGNitric Oxide
An endogenous gaseous signaling molecule which stimulates soluble guanylate cyclase and may act via S-nitrosation, nitrite/nitrate or nitrated fatty acid formation.
DRUGNitrogen
Nitrogen is the carrier gas (vehicle) for iNO. Subjects receiving placebo will receive equivalent doses of nitrogen.
Sponsors
Mallinckrodt
Cameron Dezfulian
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Masking description
Gas canisters will be marked with a bar code which will be recorded by the study coordinator and available to the study team. Only the respiratory therapy directors will be aware of the canister content (placebo vs. active drug). Treatment assignment will be revealed upon opening a sealed opaque envelope after enrollment has been confirmed.
Intervention model description
Subjects will be randomized 1:1 to either placebo or active study drug (iNO). This will be stratified within blocks of 8 subjects at each center.
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Intubated and comatose adult (\>18 yo) resuscitated from out-of-hospital cardiac arrest (OHCA)\* \*Cardiac arrest within an emergency department or outpatient medical center will be included). OHCA includes Emergency Medical Service (EMS) witnessed cardiac arrest. * Return of spontaneous circulation (ROSC) within 40 min of CPR initiation * Full Outline of Unresponsiveness (FOUR) Brainstem score ≥ 2 (i.e. patient must have pupil OR corneal reflex at the time of ED presentation or within 1h if sedation/neuromuscular blockade clouds the picture)
Exclusion criteria
* Traumatic etiology of OHCA * Prisoner * Known pregnancy (beta-human chorionic gonadotropin screening is NOT REQUIRED for enrollment in women of appropriate age) * Hemodynamic instability defined as \>1 recurrent arrest prior to enrollment OR inability to maintain mean arterial blood pressure (MAP) \> 65 using vasopressors and inotropes (ie actively up titrating medications or giving fluid bolus) * Head CT grey-white ratio \< 1.2; Head CT is NOT REQUIRED prior to enrollment * Fixed and dilated pupils without another explanation * Known intracranial hemorrhage or acute cerebral infarction; Head CT is NOT REQUIRED prior to enrollment * Malignant EEG upon presentation defined as: myoclonic status epilepticus, non-convulsive status epilepticus, generalized periodic epileptiform discharges. EEG screening is NOT REQUIRED prior to enrollment * ROSC \>3h from time of ED arrival (treatment allocation must be within 4h so anything that will prevent this is reason for exclusion) * Alert and interactive patient with minimal evidence of neurologic injury * Plan to extubate within 12 hours * Post-cardiac arrest service (PCAS) physician opinion that patient will die with \>95% likelihood. This may be based on: * Multiple medical comorbidities * Late discovery of don not resuscitate (DNR) or advanced directive * Terminal diagnosis (other than OHCA; may have caused OHCA) * Clinical judgement based on current exam and data * Patient is known to be taking phosphodiesterase type 5 (PDE5) inhibitors, soluble guanylyl cyclase (sGC) stimulator, or has a known diagnosis of Chronic thromboembolic pulmonary hypertension (CTEPH), pulmonary hypertension (PAH), or erectile dysfunction * Known enrollment in another acute interventional study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants With Death or Significant Neurological or Cardiac Impairment | Hospital discharge (+/- 3 days) | Composite of in-hospital death; OR unfavorable discharge location defined as a skilled nursing facility (SNF), long term acute care (LTAC) or hospice; OR New York Heart Association (NYHA) class III/IV heart failure at the time of discharge.\* \*In the setting of pre-existing heart failure there must be at least a 1 class decrement (eg III -\> IV). If patient was previously housed in a unfavorable destination there must be a 1 point decrement (eg from SNF to LTAC or LTAC to hospice). Subjects with pre-existing NYHA IV symptoms or living in hospice are excluded from meeting the respective outcome. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of Subjects With a Favorable Cerebral Performance Category (CPC) | Hospital discharge (+/- 3 days) | The cerebral performance category (CPC) is a standardized scale from 1-5 describing neurological and functional outcome with a long history of use in cardiac arrest trials (N Engl J Med 1986; 314:397-403). Lower scores indicate better neurological performance as follows: (1) conscious and alert with normal function or only slight disability, (2) conscious and alert with moderate disability, (3) conscious with severe disability, (4) comatose or in a persistent vegetative state, or (5) dead. CPC will be dichotomized as favorable (1, 2) or unfavorable (3-5) at designated time. |
| Number of Subjects With a Favorable Modified Rankin Score (mRS) | Hospital discharge (+/- 3 days) | The modified Rankin Score (mRS) is now recommended by consensus as the best measure of neurologic outcome in cardiac arrest studies (Circulation. 2018;137:e783-e801). The mRS runs from 0-6, where higher numbers are consistent with more severe neurologic impairment up to death (6). The scores correspond to: (0) No symptoms; (1) No significant disability. Able to carry out all usual activities, despite some symptoms.;(2) Slight disability; (3) Moderate disability; (4) Moderately severe disability; (5) Severe disability; (6) Dead. This score was dichotomized as favorable (0-3) or unfavorable (4-6) at the appointed time. |
| Number of Subjects Discharged to a Favorable Destination | Hospital discharge (+/- 3 days) | Favorable discharge destination was defined as discharge from the hospital to home or inpatient rehabilitation. Unfavorable discharge destination was defined as discharge to a skilled nursing facility, long term acute care facility, hospice or death. |
| Barthel Index (Activities of Daily Living) | Hospital discharge (+/- 3 days) | Barthel Index of Independence in Activities of Daily Living scored as a continuous 0-100 at designated time. A higher score indicates improved ability to independently perform the activities of daily living. |
| Number of Subjects Dead | Hospital discharge (+/- 3 days) | Patient declared dead at designated time point |
| Methemoglobin Level | Prior to study drug | Methemoglobin content as proportion (%) of total hemoglobin |
| Diastolic Blood Pressure | Hourly from 0 - 12 hours of study drug | Measured by arterial line |
| Systolic Blood Pressure | Hourly from 0 - 12 hours of study drug | Measured by arterial line |
| Heart Rate | Hourly from 0 - 12 hours of study drug | Calculated from continuous telemetry by monitor |
| Time to Awakening | Within 4 days of cardiac arrest | Time in hours until subject is noted to follow commands. Subjects exceeding 96 hours of coma and those that die without awakening will be designated as 100. |
Countries
United States
Participant flow
Recruitment details
All patients were enrolled in the emergency room or intensive care unit. Screening for this study began on 8/21/2017. First enrollment was 8/26/2017 and the final enrollment was 4/25/2020.
Pre-assignment details
Patients were assigned at the time of enrollment since enrollment was under exception from informed consent and all assigned patients were started on study drug.
Participants by arm
| Arm | Count |
|---|---|
| Inhaled Nitric Oxide (iNO) 20 ppm iNO delivered via mechanical ventilator connected to the iNO ventilator delivery system (iNOvent). Drug will be started as soon as possible after return of spontaneous circulation (ROSC) but no later than 4h after ROSC. Study drug will be dosed for 12h then tapered off over 1h.
Nitric Oxide: An endogenous gaseous signaling molecule which stimulates soluble guanylate cyclase and may act via S-nitrosation, nitrite/nitrate or nitrated fatty acid formation. | 30 |
| Placebo Nitrogen carrier gas delivered by identical system with similar dose/taper.
Nitrogen: Nitrogen is the carrier gas (vehicle) for iNO. Subjects receiving placebo will receive equivalent doses of nitrogen. | 27 |
| Total | 57 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 |
|---|---|---|---|
| Overall Study | Physician Decision | 0 | 1 |
Baseline characteristics
| Characteristic | Inhaled Nitric Oxide (iNO) | Placebo | Total |
|---|---|---|---|
| Age, Continuous | 65 years | 60 years | 64 years |
| Height | 171.5 centimeters | 167.8 centimeters | 170 centimeters |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 2 Participants | 0 Participants | 2 Participants |
| Race (NIH/OMB) Black or African American | 11 Participants | 5 Participants | 16 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) White | 17 Participants | 22 Participants | 39 Participants |
| Region of Enrollment United States | 30 participants | 27 participants | 57 participants |
| Sex: Female, Male Female | 12 Participants | 14 Participants | 26 Participants |
| Sex: Female, Male Male | 18 Participants | 13 Participants | 31 Participants |
| Weight | 86.6 kilograms | 81.7 kilograms | 85 kilograms |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 14 / 30 | 13 / 27 |
| other Total, other adverse events | 0 / 30 | 0 / 27 |
| serious Total, serious adverse events | 24 / 30 | 25 / 27 |
Outcome results
Primary
Number of Participants With Death or Significant Neurological or Cardiac Impairment
Composite of in-hospital death; OR unfavorable discharge location defined as a skilled nursing facility (SNF), long term acute care (LTAC) or hospice; OR New York Heart Association (NYHA) class III/IV heart failure at the time of discharge.\* \*In the setting of pre-existing heart failure there must be at least a 1 class decrement (eg III -\> IV). If patient was previously housed in a unfavorable destination there must be a 1 point decrement (eg from SNF to LTAC or LTAC to hospice). Subjects with pre-existing NYHA IV symptoms or living in hospice are excluded from meeting the respective outcome.
Time frame: Hospital discharge (+/- 3 days)
Population: All patients enrolled were followed to primary outcome consistent with FDA policies for trials conducted under exception from informed consent
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Inhaled Nitric Oxide (iNO) | Number of Participants With Death or Significant Neurological or Cardiac Impairment | 16 Participants |
| Placebo | Number of Participants With Death or Significant Neurological or Cardiac Impairment | 15 Participants |
Secondary
Barthel Index (Activities of Daily Living)
Barthel Index of Independence in Activities of Daily Living scored as a continuous 0-100 at designated time. A higher score indicates improved ability to independently perform the activities of daily living.
Time frame: 90 days after cardiac arrest (+/- 3 days)
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Inhaled Nitric Oxide (iNO) | Barthel Index (Activities of Daily Living) | 100 score on a scale |
| Placebo | Barthel Index (Activities of Daily Living) | 100 score on a scale |
Secondary
Barthel Index (Activities of Daily Living)
Barthel Index of Independence in Activities of Daily Living scored as a continuous 0-100 at designated time. A higher score indicates improved ability to independently perform the activities of daily living.
Time frame: Hospital discharge (+/- 3 days)
Population: One surviving subject in placebo group withdrew consent before discharge and was therefore not assessed.
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Inhaled Nitric Oxide (iNO) | Barthel Index (Activities of Daily Living) | 70 score on a scale |
| Placebo | Barthel Index (Activities of Daily Living) | 65 score on a scale |
Secondary
Barthel Index (Activities of Daily Living)
Barthel Index of Independence in Activities of Daily Living scored as a continuous 0-100 at designated time. A higher score indicates improved ability to independently perform the activities of daily living.
Time frame: 30 days after cardiac arrest (+/- 3 days)
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Inhaled Nitric Oxide (iNO) | Barthel Index (Activities of Daily Living) | 100 score on a scale |
| Placebo | Barthel Index (Activities of Daily Living) | 95 score on a scale |
Secondary
Diastolic Blood Pressure
Measured by arterial line
Time frame: Hourly from 0 - 12 hours of study drug
Population: Missing values occurred due to death during study drug (iNO, 2; placebo, 1), withdrawal of consent (iNO, 1; placebo, 1), termination of study by PI and subsequent death (placebo, 1), procedures outside the ICU (placebo, 1), arterial line delay or malfunction (iNO, 1; placebo, 2).
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Inhaled Nitric Oxide (iNO) | Diastolic Blood Pressure | 2 hours after study drug | 72.1 mm Hg | Standard Deviation 3.3 |
| Inhaled Nitric Oxide (iNO) | Diastolic Blood Pressure | 7 hours after study drug | 68.7 mm Hg | Standard Deviation 3.8 |
| Inhaled Nitric Oxide (iNO) | Diastolic Blood Pressure | 4 hours after study drug | 71.6 mm Hg | Standard Deviation 2.4 |
| Inhaled Nitric Oxide (iNO) | Diastolic Blood Pressure | 8 hours after study drug | 71.5 mm Hg | Standard Deviation 2.4 |
| Inhaled Nitric Oxide (iNO) | Diastolic Blood Pressure | 1 hour after study drug | 72.5 mm Hg | Standard Deviation 4.6 |
| Inhaled Nitric Oxide (iNO) | Diastolic Blood Pressure | 9 hours after study drug | 70.8 mm Hg | Standard Deviation 3.3 |
| Inhaled Nitric Oxide (iNO) | Diastolic Blood Pressure | 5 hours after study drug | 72.6 mm Hg | Standard Deviation 3.7 |
| Inhaled Nitric Oxide (iNO) | Diastolic Blood Pressure | 10 hours after study drug | 71.4 mm Hg | Standard Deviation 2.3 |
| Inhaled Nitric Oxide (iNO) | Diastolic Blood Pressure | 3 hours after study drug | 71.3 mm Hg | Standard Deviation 2.7 |
| Inhaled Nitric Oxide (iNO) | Diastolic Blood Pressure | 11 hours after study drug | 70.7 mm Hg | Standard Deviation 2.9 |
| Inhaled Nitric Oxide (iNO) | Diastolic Blood Pressure | 6 hours after study drug | 74.9 mm Hg | Standard Deviation 2.7 |
| Inhaled Nitric Oxide (iNO) | Diastolic Blood Pressure | 12 hours after study drug | 67.0 mm Hg | Standard Deviation 2.3 |
| Inhaled Nitric Oxide (iNO) | Diastolic Blood Pressure | Time zero (immediately before study drug) | 75.1 mm Hg | Standard Deviation 2.8 |
| Placebo | Diastolic Blood Pressure | 12 hours after study drug | 66.6 mm Hg | Standard Deviation 3.2 |
| Placebo | Diastolic Blood Pressure | Time zero (immediately before study drug) | 67.3 mm Hg | Standard Deviation 3.7 |
| Placebo | Diastolic Blood Pressure | 1 hour after study drug | 67.3 mm Hg | Standard Deviation 2.2 |
| Placebo | Diastolic Blood Pressure | 2 hours after study drug | 67.0 mm Hg | Standard Deviation 4.2 |
| Placebo | Diastolic Blood Pressure | 3 hours after study drug | 67.0 mm Hg | Standard Deviation 2.3 |
| Placebo | Diastolic Blood Pressure | 4 hours after study drug | 68.1 mm Hg | Standard Deviation 3.6 |
| Placebo | Diastolic Blood Pressure | 5 hours after study drug | 62.9 mm Hg | Standard Deviation 2.2 |
| Placebo | Diastolic Blood Pressure | 6 hours after study drug | 67.8 mm Hg | Standard Deviation 3.1 |
| Placebo | Diastolic Blood Pressure | 7 hours after study drug | 66.5 mm Hg | Standard Deviation 4.1 |
| Placebo | Diastolic Blood Pressure | 8 hours after study drug | 65.5 mm Hg | Standard Deviation 3.5 |
| Placebo | Diastolic Blood Pressure | 9 hours after study drug | 62.9 mm Hg | Standard Deviation 2.3 |
| Placebo | Diastolic Blood Pressure | 10 hours after study drug | 66.4 mm Hg | Standard Deviation 3.7 |
| Placebo | Diastolic Blood Pressure | 11 hours after study drug | 61.5 mm Hg | Standard Deviation 2 |
Secondary
Heart Rate
Calculated from continuous telemetry by monitor
Time frame: Hourly from 0 - 12 hours of study drug
Population: Missing values occurred due to death during study drug (iNO, 2; placebo, 1), withdrawal of consent (iNO, 1; placebo, 1), termination of study by PI (placebo, 1), procedures outside the ICU (placebo, 1).
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Inhaled Nitric Oxide (iNO) | Heart Rate | 2 hours after study drug start | 84.4 beats per minute | Standard Deviation 3.2 |
| Inhaled Nitric Oxide (iNO) | Heart Rate | 7 hours after study drug start | 76.8 beats per minute | Standard Deviation 3.3 |
| Inhaled Nitric Oxide (iNO) | Heart Rate | 4 hours after study drug start | 77.1 beats per minute | Standard Deviation 3 |
| Inhaled Nitric Oxide (iNO) | Heart Rate | 8 hours after study drug start | 76.1 beats per minute | Standard Deviation 3.9 |
| Inhaled Nitric Oxide (iNO) | Heart Rate | 1 hour after study drug start | 85.2 beats per minute | Standard Deviation 3.6 |
| Inhaled Nitric Oxide (iNO) | Heart Rate | 9 hours after study drug start | 75.9 beats per minute | Standard Deviation 4 |
| Inhaled Nitric Oxide (iNO) | Heart Rate | 5 hours after study drug start | 78.0 beats per minute | Standard Deviation 2.9 |
| Inhaled Nitric Oxide (iNO) | Heart Rate | 10 hours after study drug start | 74.7 beats per minute | Standard Deviation 3.9 |
| Inhaled Nitric Oxide (iNO) | Heart Rate | 3 hours after study drug start | 82.3 beats per minute | Standard Deviation 3.3 |
| Inhaled Nitric Oxide (iNO) | Heart Rate | 11 hours after study drug start | 72.9 beats per minute | Standard Deviation 3.8 |
| Inhaled Nitric Oxide (iNO) | Heart Rate | 6 hours after study drug start | 76.7 beats per minute | Standard Deviation 3.1 |
| Inhaled Nitric Oxide (iNO) | Heart Rate | 12 hours after study drug start | 73.4 beats per minute | Standard Deviation 3.5 |
| Inhaled Nitric Oxide (iNO) | Heart Rate | 0 hour (immediately before study drug) | 90.0 beats per minute | Standard Deviation 3.8 |
| Placebo | Heart Rate | 12 hours after study drug start | 75.9 beats per minute | Standard Deviation 4.1 |
| Placebo | Heart Rate | 0 hour (immediately before study drug) | 31.1 beats per minute | Standard Deviation 3.4 |
| Placebo | Heart Rate | 1 hour after study drug start | 91.8 beats per minute | Standard Deviation 5.5 |
| Placebo | Heart Rate | 2 hours after study drug start | 85.7 beats per minute | Standard Deviation 4.5 |
| Placebo | Heart Rate | 3 hours after study drug start | 85.9 beats per minute | Standard Deviation 4.6 |
| Placebo | Heart Rate | 4 hours after study drug start | 83.6 beats per minute | Standard Deviation 4.3 |
| Placebo | Heart Rate | 5 hours after study drug start | 79.8 beats per minute | Standard Deviation 4.2 |
| Placebo | Heart Rate | 6 hours after study drug start | 77.5 beats per minute | Standard Deviation 4 |
| Placebo | Heart Rate | 7 hours after study drug start | 74.9 beats per minute | Standard Deviation 3.5 |
| Placebo | Heart Rate | 8 hours after study drug start | 76.0 beats per minute | Standard Deviation 3.6 |
| Placebo | Heart Rate | 9 hours after study drug start | 75.0 beats per minute | Standard Deviation 3.9 |
| Placebo | Heart Rate | 10 hours after study drug start | 75.4 beats per minute | Standard Deviation 3.2 |
| Placebo | Heart Rate | 11 hours after study drug start | 75.7 beats per minute | Standard Deviation 3.5 |
Secondary
Methemoglobin Level
Methemoglobin content as proportion (%) of total hemoglobin
Time frame: 12 hours after study drug initiated
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Inhaled Nitric Oxide (iNO) | Methemoglobin Level | 0.8 percentage of hemoglobin |
| Placebo | Methemoglobin Level | 0.3 percentage of hemoglobin |
Secondary
Methemoglobin Level
Methemoglobin content as proportion (%) of total hemoglobin
Time frame: Prior to study drug
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Inhaled Nitric Oxide (iNO) | Methemoglobin Level | 0.1 percentage of hemoglobin |
| Placebo | Methemoglobin Level | 0.2 percentage of hemoglobin |
Secondary
Methemoglobin Level
Methemoglobin content as proportion (%) of total hemoglobin
Time frame: 6 hours after study drug initiated
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Inhaled Nitric Oxide (iNO) | Methemoglobin Level | 1.1 percentage of hemoglobin |
| Placebo | Methemoglobin Level | 0.5 percentage of hemoglobin |
Secondary
Number of Subjects Dead
Patient declared dead at designated time point
Time frame: 90 days after cardiac arrest (+/- 3 days)
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Inhaled Nitric Oxide (iNO) | Number of Subjects Dead | 14 Participants |
| Placebo | Number of Subjects Dead | 13 Participants |
Secondary
Number of Subjects Dead
Patient declared dead at designated time point
Time frame: Hospital discharge (+/- 3 days)
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Inhaled Nitric Oxide (iNO) | Number of Subjects Dead | 13 Participants |
| Placebo | Number of Subjects Dead | 11 Participants |
Secondary
Number of Subjects Dead
Patient declared dead at designated time point
Time frame: 30 days after cardiac arrest (+/- 3 days)
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Inhaled Nitric Oxide (iNO) | Number of Subjects Dead | 14 Participants |
| Placebo | Number of Subjects Dead | 12 Participants |
Secondary
Number of Subjects Discharged to a Favorable Destination
Favorable discharge destination was defined as discharge from the hospital to home or inpatient rehabilitation. Unfavorable discharge destination was defined as discharge to a skilled nursing facility, long term acute care facility, hospice or death.
Time frame: Hospital discharge (+/- 3 days)
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Inhaled Nitric Oxide (iNO) | Number of Subjects Discharged to a Favorable Destination | 15 Participants |
| Placebo | Number of Subjects Discharged to a Favorable Destination | 12 Participants |
Secondary
Number of Subjects With a Favorable Cerebral Performance Category (CPC)
The cerebral performance category (CPC) is a standardized scale from 1-5 describing neurological and functional outcome with a long history of use in cardiac arrest trials (N Engl J Med 1986; 314:397-403). Lower scores indicate better neurological performance as follows: (1) conscious and alert with normal function or only slight disability, (2) conscious and alert with moderate disability, (3) conscious with severe disability, (4) comatose or in a persistent vegetative state, or (5) dead. CPC will be dichotomized as favorable (1, 2) or unfavorable (3-5) at designated time.
Time frame: Hospital discharge (+/- 3 days)
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Inhaled Nitric Oxide (iNO) | Number of Subjects With a Favorable Cerebral Performance Category (CPC) | 11 Participants |
| Placebo | Number of Subjects With a Favorable Cerebral Performance Category (CPC) | 7 Participants |
Secondary
Number of Subjects With a Favorable Cerebral Performance Category (CPC)
The cerebral performance category (CPC) is a standardized scale from 1-5 describing neurological and functional outcome with a long history of use in cardiac arrest trials (N Engl J Med 1986; 314:397-403). Lower scores indicate better neurological performance as follows: (1) conscious and alert with normal function or only slight disability, (2) conscious and alert with moderate disability, (3) conscious with severe disability, (4) comatose or in a persistent vegetative state, or (5) dead. CPC will be dichotomized as favorable (1, 2) or unfavorable (3-5) at designated time.
Time frame: 30 days after cardiac arrest (+/- 3 days)
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Inhaled Nitric Oxide (iNO) | Number of Subjects With a Favorable Cerebral Performance Category (CPC) | 8 Participants |
| Placebo | Number of Subjects With a Favorable Cerebral Performance Category (CPC) | 9 Participants |
Secondary
Number of Subjects With a Favorable Cerebral Performance Category (CPC)
The cerebral performance category (CPC) is a standardized scale from 1-5 describing neurological and functional outcome with a long history of use in cardiac arrest trials (N Engl J Med 1986; 314:397-403). Lower scores indicate better neurological performance as follows: (1) conscious and alert with normal function or only slight disability, (2) conscious and alert with moderate disability, (3) conscious with severe disability, (4) comatose or in a persistent vegetative state, or (5) dead. CPC will be dichotomized as favorable (1, 2) or unfavorable (3-5) at designated time.
Time frame: 90 days after cardiac arrest (+/- 3 days)
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Inhaled Nitric Oxide (iNO) | Number of Subjects With a Favorable Cerebral Performance Category (CPC) | 10 Participants |
| Placebo | Number of Subjects With a Favorable Cerebral Performance Category (CPC) | 8 Participants |
Secondary
Number of Subjects With a Favorable Modified Rankin Score (mRS)
The modified Rankin Score (mRS) is now recommended by consensus as the best measure of neurologic outcome in cardiac arrest studies (Circulation. 2018;137:e783-e801). The mRS runs from 0-6, where higher numbers are consistent with more severe neurologic impairment up to death (6). The scores correspond to: (0) No symptoms; (1) No significant disability. Able to carry out all usual activities, despite some symptoms.;(2) Slight disability; (3) Moderate disability; (4) Moderately severe disability; (5) Severe disability; (6) Dead. This score was dichotomized as favorable (0-3) or unfavorable (4-6) at the appointed time.
Time frame: Hospital discharge (+/- 3 days)
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Inhaled Nitric Oxide (iNO) | Number of Subjects With a Favorable Modified Rankin Score (mRS) | 11 Participants |
| Placebo | Number of Subjects With a Favorable Modified Rankin Score (mRS) | 7 Participants |
Secondary
Number of Subjects With a Favorable Modified Rankin Score (mRS)
The modified Rankin Score (mRS) is now recommended by consensus as the best measure of neurologic outcome in cardiac arrest studies (Circulation. 2018;137:e783-e801). The mRS runs from 0-6, where higher numbers are consistent with more severe neurologic impairment up to death (6). The scores correspond to: (0) No symptoms; (1) No significant disability. Able to carry out all usual activities, despite some symptoms.;(2) Slight disability; (3) Moderate disability; (4) Moderately severe disability; (5) Severe disability; (6) Dead. This score was dichotomized as favorable (0-3) or unfavorable (4-6) at the appointed time.
Time frame: 30 days after cardiac arrest (+/- 3 days)
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Inhaled Nitric Oxide (iNO) | Number of Subjects With a Favorable Modified Rankin Score (mRS) | 9 Participants |
| Placebo | Number of Subjects With a Favorable Modified Rankin Score (mRS) | 10 Participants |
Secondary
Number of Subjects With a Favorable Modified Rankin Score (mRS)
The modified Rankin Score (mRS) is now recommended by consensus as the best measure of neurologic outcome in cardiac arrest studies (Circulation. 2018;137:e783-e801). The mRS runs from 0-6, where higher numbers are consistent with more severe neurologic impairment up to death (6). The scores correspond to: (0) No symptoms; (1) No significant disability. Able to carry out all usual activities, despite some symptoms.;(2) Slight disability; (3) Moderate disability; (4) Moderately severe disability; (5) Severe disability; (6) Dead. This score was dichotomized as favorable (0-3) or unfavorable (4-6) at the appointed time.
Time frame: 90 days after cardiac arrest (+/- 3 days)
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Inhaled Nitric Oxide (iNO) | Number of Subjects With a Favorable Modified Rankin Score (mRS) | 11 Participants |
| Placebo | Number of Subjects With a Favorable Modified Rankin Score (mRS) | 9 Participants |
Secondary
Systolic Blood Pressure
Measured by arterial line
Time frame: Hourly from 0 - 12 hours of study drug
Population: Missing values occurred due to death during study drug (iNO, 2; placebo, 1), withdrawal of consent (iNO, 1; placebo, 1), termination of study by PI and subsequent death (placebo, 1), procedures outside the ICU (placebo, 1), arterial line delay or malfunction (iNO, 1; placebo, 2).
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Inhaled Nitric Oxide (iNO) | Systolic Blood Pressure | 2 hours after study drug | 132.2 mm Hg | Standard Deviation 5.2 |
| Inhaled Nitric Oxide (iNO) | Systolic Blood Pressure | 7 hours after study drug | 129.0 mm Hg | Standard Deviation 3.8 |
| Inhaled Nitric Oxide (iNO) | Systolic Blood Pressure | 4 hours after study drug | 135.3 mm Hg | Standard Deviation 4.5 |
| Inhaled Nitric Oxide (iNO) | Systolic Blood Pressure | 8 hours after study drug | 126.0 mm Hg | Standard Deviation 4 |
| Inhaled Nitric Oxide (iNO) | Systolic Blood Pressure | 1 hour after study drug | 141.1 mm Hg | Standard Deviation 6.6 |
| Inhaled Nitric Oxide (iNO) | Systolic Blood Pressure | 9 hours after study drug | 125.9 mm Hg | Standard Deviation 3.9 |
| Inhaled Nitric Oxide (iNO) | Systolic Blood Pressure | 5 hours after study drug | 131.4 mm Hg | Standard Deviation 3.9 |
| Inhaled Nitric Oxide (iNO) | Systolic Blood Pressure | 10 hours after study drug | 127.1 mm Hg | Standard Deviation 3.8 |
| Inhaled Nitric Oxide (iNO) | Systolic Blood Pressure | 3 hours after study drug | 138.9 mm Hg | Standard Deviation 5.3 |
| Inhaled Nitric Oxide (iNO) | Systolic Blood Pressure | 11 hours after study drug | 119.4 mm Hg | Standard Deviation 3.7 |
| Inhaled Nitric Oxide (iNO) | Systolic Blood Pressure | 6 hours after study drug | 126.2 mm Hg | Standard Deviation 4 |
| Inhaled Nitric Oxide (iNO) | Systolic Blood Pressure | 12 hours after study drug | 119.4 mm Hg | Standard Deviation 3.7 |
| Inhaled Nitric Oxide (iNO) | Systolic Blood Pressure | 0 hour (immediately before study drug start) | 143.1 mm Hg | Standard Deviation 6.6 |
| Placebo | Systolic Blood Pressure | 12 hours after study drug | 134.2 mm Hg | Standard Deviation 6.3 |
| Placebo | Systolic Blood Pressure | 0 hour (immediately before study drug start) | 140.0 mm Hg | Standard Deviation 7.6 |
| Placebo | Systolic Blood Pressure | 1 hour after study drug | 136.1 mm Hg | Standard Deviation 7.3 |
| Placebo | Systolic Blood Pressure | 2 hours after study drug | 140.5 mm Hg | Standard Deviation 6.5 |
| Placebo | Systolic Blood Pressure | 3 hours after study drug | 132.5 mm Hg | Standard Deviation 5.8 |
| Placebo | Systolic Blood Pressure | 4 hours after study drug | 134.3 mm Hg | Standard Deviation 5.3 |
| Placebo | Systolic Blood Pressure | 5 hours after study drug | 134. mm Hg | Standard Deviation 5.3 |
| Placebo | Systolic Blood Pressure | 6 hours after study drug | 139.8 mm Hg | Standard Deviation 5.9 |
| Placebo | Systolic Blood Pressure | 7 hours after study drug | 128.8 mm Hg | Standard Deviation 6.1 |
| Placebo | Systolic Blood Pressure | 8 hours after study drug | 132.2 mm Hg | Standard Deviation 6 |
| Placebo | Systolic Blood Pressure | 9 hours after study drug | 132.5 mm Hg | Standard Deviation 6.2 |
| Placebo | Systolic Blood Pressure | 10 hours after study drug | 136.8 mm Hg | Standard Deviation 5.9 |
| Placebo | Systolic Blood Pressure | 11 hours after study drug | 136.7 mm Hg | Standard Deviation 5 |
Secondary
Time to Awakening
Time in hours until subject is noted to follow commands. Subjects exceeding 96 hours of coma and those that die without awakening will be designated as 100.
Time frame: Within 4 days of cardiac arrest
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Inhaled Nitric Oxide (iNO) | Time to Awakening | 47.5 hours |
| Placebo | Time to Awakening | 25 hours |