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Phrenic Nerve Block to Mitigate Self-inflicted Lung Injury

Feasibility of Phrenic Nerve Block to Mitigate Self-inflicted Lung Injury in ARF Patients Under Mechanical Ventilation on Spontaneous Breathing

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03978845
Enrollment
10
Registered
2019-06-07
Start date
2019-05-15
Completion date
2020-09-09
Last updated
2020-09-30

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

Conditions

Mechanical Ventilation, Respiratory Failure

Brief summary

The purpose of this single-centered, proof of concept study is to determine whether it is feasible to perform a phrenic nerve block to reduce diaphragm electrical activity and, therefore, inspiratory effort and if such block reduces self-inflicted lung injury on patients under mechanical ventilation on spontaneous breathing. Ten patients will be monitored with electrical impedance tomography, NAVA catheter, and esophageal balloon. Using a nerve stimulator and an ultrasound, we will identify the phrenic nerve on its cervical portion bilaterally and administer perineural low-dose lidocaine. Diaphragm electrical activity, transpulmonary pressure and data on ventilation distribution will be continuously collected. The study will be over once the patient presents the same diaphragm electrical activity and transpulmonary pressure as before the phrenic nerve block.

Detailed description

The use of protective mechanical ventilation has improved prognosis on patients with Acute Respiratory Failure. The association of neuromuscular blockade in the first 48-72h has additionally contributed to a higher survival rate. Such improvement may be due to the reduction of transpulmonary pressures caused by the patient's inspiratory effort. To achieve appropriate neuromuscular blockade, highes doses of both neuromuscular blocking agents and sedatives are required. Therefore, such a strategy usually causes muscular atrophy, including the diaphragm. Because of the augmented neural drive of such patients, exacerbated by inflammation and pulmonary edema, the consequent high tidal volume and transpulmonary pressure cannot be reduced by the newest sedatives. In fact, some of these sedatives may even deteriorate ventilatory dyssynchrony. Our intention is to verify a novel approach: whether is possible to reduce the inspiratory effort of patients without the use of systemic neuromuscular blocking agents. Our objective in this proof of concept study is to determine the feasibility the use of phrenic nerve blockade to decrease transpulmonary pressure and tidal volume, as well as quantify its effects on esophageal pressure, diaphragmatic electrical activity, transpulmonary pressure and ventilation distribution in patients on spontaneous breathing. It is expected that such intervention will reduce diaphragm electrical activity, leading to lower transpulmonary pressure, tidal volume and driving pressures. All patients will be submitted to the same intervention. Respiratory mechanics, ventilation distribution, diaphragm electrical activity, heart rate, mean arterial pressure and peripheral saturation will be collected throughout the study. Once the patient presents the same diaphragmatic electrical activity and transpulmonary pressure as before the phrenic nerve block, the study will be over.

Interventions

DRUGLidocaine

Using an ultrasound and a nerve stimulator, the phrenic nerve will be identified and low-dose lidocaine will be administered perineurally.

Sponsors

University of Sao Paulo General Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

All patients will be submitted to the same procedures. There will be no between-group comparisons.

Eligibility

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

Inclusion criteria

* Age \> 17 years-old; * Under mechanical ventilation on spontaneous breathing, capable of triggering the ventilator with P/F \< 300; * Tidal volume \> 10ml/kg with inspiratory pressure of 12 cmH2O OR driving pressure \> 15 cm H2O with inspiratory pressure of 12 cmH2O

Exclusion criteria

* Use of neuromuscular blocking agents less than 3h; * Richmond Agitation-Sedation Scale (RASS) \> 0; * Arterial pH \< 7.25; * Hemodynamically unstable or with increasing doses of vasopressors in the last 2h; * Intracranial hypertension; * Thoracic or abdominal tubes; * Any neuromuscular disease; * Spinal injury; * Ascitis; * Thoracic burn injury; * Tetanus; * Pregnancy.

Design outcomes

Primary

MeasureTime frameDescription
Reduction of tidal volume or transpulmonary pressure20 minutesTidal volume or transpulmonary pressure measured using EIT, Servo-I and an esophageal balloon

Secondary

MeasureTime frameDescription
Reduction of the inspiratory effort20 minutes - 3 hoursDiaphragm electrical activity using NAVA
Consequences on mechanical ventilation20 minutes - 3 hoursTidal volume, pendellfut and asynchronies measured by EIT
Time to complete weaning of the blockade30 minutes - 3 hoursPatients will be monitored until full recover of inspiratory effort or diaphragm electrical activity

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026