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Targeted Therapeutic Mild Hypercapnia After Resuscitated Cardiac Arrest

TAME Cardiac Arrest Trial: Targeted Therapeutic Mild Hypercapnia After Resuscitated Cardiac Arrest: A Phase III Multi-Centre Randomised Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03114033
Acronym
TAME
Enrollment
1700
Registered
2017-04-14
Start date
2018-02-15
Completion date
2022-12-31
Last updated
2022-04-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Out-Of-Hospital Cardiac Arrest

Keywords

Cardiac Arrest, Intensive Care Unit, Therapeutic Mild Hypercapnia, Normocapnia, Mortality, Neurological function

Brief summary

The TAME Cardiac Arrest trial will study the ability of higher arterial carbon dioxide (PaCO2) levels to reduce brain damage, comparing giving patients 'normal' to 'slightly higher than normal' blood PaCO2 levels and assessing their ability to return to normal life-tasks. It will be the largest trial ever conducted in heart attack patients in the intensive care unit. This therapy is cost free and, if shown to be effective, will improve thousands of lives, transform clinical practice, and yield major savings.

Detailed description

Cardiac arrest is a common and catastrophic event with substantial human and financial costs. It is well understood that cardiac arrest leads to brain injury. However, what is not widely appreciated is that, after circulation has been restored, cerebral hypoperfusion continues. Ongoing cerebral vasoconstriction and cerebral hypoxia has been demonstrated using technologies that include positron emission tomography, ultrasound, jugular bulb oxygen saturation and cerebral oximetry. A likely mechanism responsible for sustained early cerebral hypoperfusion relates to impaired cerebrovascular auto-regulation. Such impaired cerebral auto-regulation may make even a normal arterial carbon dioxide tension (PaCO2) (the major physiological regulator of cerebral blood flow) insufficient to achieve and maintain adequate cerebral perfusion and, consequently, cerebral oxygenation. However, PaCO2 is the major determinant of cerebral blood flow and an increased PaCO2 (hypercapnia) markedly increases cerebral blood flow. Moreover, arterial carbon dioxide is modifiable and, as such, is a potential therapeutic target. The TAME Cardiac Arrest Trial is a definitive phase III multi-centre randomised controlled trial in resuscitated cardiac arrest patients. This trial will determine whether targeted therapeutic mild hypercapnia (TTMH) applied during the first 24 hours of mechanical ventilation in the intensive care unit (ICU) improves neurological outcome at 6 months compared to standard care (targeted normocapnia (TN). Supported by compelling preliminary data, significant improvements in patient outcomes are achievable with this proposed simple and cost free therapy. Recruiting 1,700 patients, for multiple sites in many countries, this will be the largest trial ever conducted involving resuscitated cardiac arrest patients admitted to the ICU. If the TAME Cardiac Arrest Trial confirms that TTMH is effective, its findings will improve the lives of many, transform clinical practice and yield major economic gains worldwide.

Interventions

OTHERTargeted therapeutic mild hypercapnia

Patients allocated to the TTMH protocol will be sedated to achieve moderate to deep sedation (a target Richmond Agitation Scale Score of -4). Arterial blood gases and end- tidal carbon dioxide levels will be measured at baseline and then used to guide respiratory rate adjustments of minute ventilation to remain within the target PaCO2 range of 50-55 mmHg. Arterial blood gases will be repeated every 4 hours for 24 hours following randomisation or if end-tidal carbon dioxide values change \>5 mmHg

OTHERTargeted normocapnia (Standard care)

Patients allocated to the standard care (TN) protocol will be managed according to current practice and in accordance with ILCOR guidelines which recommend maintaining normocapnia in these patients. They will be sedated to achieve moderate to deep sedation (a target Richmond Agitation Scale Score of - 4). Arterial blood gases and end-tidal carbon dioxide levels will be measured at baseline and then used to guide respiratory rate adjustments of minute ventilation to remain within the target PaCO2 range of 35-45 mmHg. Arterial blood gases will be repeated every 4 hours for 24 hours following randomisation or if end-tidal carbon dioxide values change \>5 mmHg.

Sponsors

National Health and Medical Research Council, Australia
CollaboratorOTHER
Health Research Board, Ireland
CollaboratorOTHER
Australian and New Zealand Intensive Care Research Centre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Masking description

A Randomised, Parallel Groups, Assessor Blinded, Clinical Trial

Intervention model description

Parallel assignment

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult (age ≥18 years or older) * Out-of-hospital cardiac arrest of a presumed cardiac or unknown cause * Sustained ROSC - defined as 20 minutes with signs of circulation without the need for chest compressions * Unconscious (FOUR-score motor response of \<4, not able to obey verbal commands after sustained ROSC) (Appendix D) * Eligible for intensive care without restrictions or limitations * Within \<180 minutes of ROSC

Exclusion criteria

* Unwitnessed cardiac arrest with an initial rhythm of asystole * Temperature on admission \<30oC * On ECMO prior to ROSC * Obvious or suspected pregnancy * Intracranial bleeding * Severe chronic obstructive pulmonary disorder (COPD) with long-term home oxygen therapy

Design outcomes

Primary

MeasureTime frameDescription
Neurological outcome6 months following enrolmentProportion of patients with a favourable (score ≥5) neurological outcome as assessed using the Glasgow Outcomes Score Extended (GOSE) method.

Secondary

MeasureTime frameDescription
Mortality at intensive care unit discharge6 months after randomisationMortality at intensive care unit discharge
Mortality at hospital discharge6 months after randomisationMortality at hospital discharge
Health-related Quality of Life (EQ-5D-5L)6 months after randomisationHealth-related Quality of Life (EQ-5D-5L) at 6 months
modified Rankin scale (mRS)6 months after randomisationmodified Rankin scale (mRS) with favourable score of equal to or less than 3
Montreal Cognitive Assessment (MoCA-blind)6 months after randomisationMontreal Cognitive Assessment (MoCA-blind) at 6 months
Mortality at 6 months6 months after randomisationMortality at 6 months
Informant Questionnaire on Cognitive Decline in the Elderly-Cardiac Arrest (IQCODE)6 months after randomisationIQCODE
Symbol Digit Modality Test6 months after randomisationSDMT at 6 months

Other

MeasureTime frameDescription
Health economic evaluation6 months after randomisationEvaluation of hospital and post-discharge estimates of costs at 6 months
PneumoniaOccurring from enrolment until Day 7 while the participant is in the intensive care unit as reported by treating clinicians.Pneumonia as defined by the presence of increased or purulent trachael secretions, new or progressive radiographic infiltrate and a decreased arterial oxygen tension fraction of inspired oxygen ratio of less than 240 mmHg or less than 32 kPa
Sepsis and septic shockOccurring from enrolment until Day 7 while the participant is in the intensive care unit as reported by treating clinicians.Sepsis and septic shock according to the third international consensus definitions for sepsis and septic shock as published in the journal JAMA 2016;315:801-810
BradycardiaOccurring from enrolment until Day 7 while the participant is in the intensive care unit as reported by treating clinicians.Bradycardia requiring pacing
Moderate or severe bleedingOccurring from enrolment until Day 7 while the participant is in the intensive care unit as reported by treating clinicians.Moderate or severe bleeding according to the GUSTO criteria as reported in the journal N Engl J Med 1993;329:673-82
Cooling device-related skin complicationsOccurring from enrolment until Day 7 while the participant is in the intensive care unit as reported by treating clinicians.Cooling device-related skin complications as defined as being blistering or skin necrosis in areas covered by surface device.
ArrhythmiaOccurring from enrolment until Day 7 while the participant is in the intensive care unit as reported by treating clinicians.Arrhythmia that results in haemodynamic compromise (for example ventricular fibrillation and ventricular tachycardia).
Quality Adjust Life Years (QALYs)6 months after randomisationQuality Adjust Life Years (QALYs)

Countries

Australia, Belgium, Denmark, Finland, France, Ireland, Italy, Netherlands, New Zealand, Norway, Saudi Arabia, Slovenia, Sweden, United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 5, 2026