Royal Columbian Hospital
New Westminster, B.C., V3L 3W7, Canada
NCT Number: NCT07505589
The goal of this clinical trial is to test the feasibility of pacing the phrenic nerve to stimulate the diaphragm in order to improve the lung function in brain dead organ donors. The main questions it aims to answer are:
* Proof of concept and feasibility * Can lung function be improved in lungs that have been disqualified for donation
Participants will have an AeroPace catheter inserted and will be paced on every breath up to the time of organ donation.
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Notify Me19 year–100 year
All sexes
Interventional
Not applicable
New Westminster, B.C., V3L 3W7, Canada
Single-center, single-arm, proof-of-concept trial. Up to twenty (20) subjects on mechanical ventilation who are determined to be brain dead and whose lungs are declined for donation based on a PaO2/FiO2 ratio < 300 mmHg will be enrolled. Subjects may also be enrolled in the study at the request of the donation team if the lungs are accepted for donation but of marginal quality. Consent from the temporary substitute decision maker (TSDM) will be obtained for (i) organ donation and (ii) for study participation.
All subjects will receive Lungpacer AeroPace Protect System catheter-based transvenous phrenic nerve stimulation (LAPS-PNS) with lung-protective mechanical ventilation and standard of care for transplant donors. Insertion of the AeroPace Catheter will be conducted as soon as possible after the determination of lung transplant ineligibility. LAPS-PNS will be titrated with the ventilator to provide a contribution to the work of breathing sufficient to retain diaphragm activation.
Measurements to determine the effects of LAPS-PNS on donor lung function and physiology will be conducted until the time of organ donation. An esophageal-gastric manometer and electrical impedance tomography (EIT) unit will be utilized, respectively, to assess transdiaphragmatic pressure and lung volume distribution. Data collected for brain dead donors admitted to the same ICU over the 2 years preceding the study start who did not qualify for lung donation will serve as an unmatched comparator group.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Diaphragm neurostimulation device for phrenic nerve pacing during mechanical ventilation.
Time frame: ABG measurements will be taken every 6 hours from enrolment until study endpoint for each participant.
PaO2/FiO2 ratio measured from arterial blood gas values.
Time frame: Under continuous observation from subject enrolment until study endpoint (organ donation), an average of 40 hours.
Determine whether any unexpected, or device-related or procedure-related complications occur in brain dead subjects. Standardized checklists will be developed to track safety events including arrhythmia, bradycardia, discomfort, hypertension/hypotension, inappropriate stimulation, pain or discomfort, phrenic nerve damage or injury, and syncope.
Time frame: Under continuous observation from subject enrolment until study endpoint (organ donation), an average of 40 hours.
Eligible breaths are defined as those breaths in which PNS is not precluded by clinical care/procedures or subject transport.
Time frame: Under continuous observation from subject enrolment until study endpoint (organ donation), an average of 40 hours.
Measured in impedance units, percentage change from baseline
Time frame: Under continuous observation from subject enrolment until study endpoint (organ donation), an average of 40 hours.
Time frame: Under continuous observation from subject enrolment until study endpoint (organ donation), an average of 40 hours.
Time frame: Under continuous observation from subject enrolment until study endpoint (organ donation), an average of 40 hours.
Measures of urine output (mL/kg) and creatinine (umol/L)
Time frame: Under continuous observation from subject enrolment until study endpoint (organ donation), an average of 40 hours.
Collection variables include temperature (degrees celsius), heart rate (bpm), SBP/DBP, MAP, RR (breaths/min)
Fraser Health
Other
Diaphragm Neurostimulation to Improve Lung Function in Brain Dead Donors
Acronym: POD
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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