Partial Neuromuscular Blockade in Acute Respiratory Distress Syndrome

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

PNEUMA is a preliminary safety and feasibility trial of a novel approach to the titration of neuromuscular blockade (NMB) to safe spontaneous breathing in patients with severe acute respiratory distress syndrome (ARDS) supported with veno-venous extracorporeal membrane oxygenation (VV-ECMO).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Potentially injurious respiratory efforts as defined by esophageal pressure swings or occlusion pressure swing AND Riker Sedation-Agitation Scale (SAS) ≤2 (if the clinical team has elected to sedate to that depth).

• The medical team has undertaken a trial of discontinuing neuromuscular blockade and determined that the patient requires reinstitution of neuromuscular blockade to ensure toleration of ECMO and they are willing for the patient undergo a trial of partial neuromuscular blockade

• The patient is receiving neuromuscular blockade with no plan to discontinue neuromuscular blockade until the next day and the medical team is willing for the patient to undergo a trial of partial neuromuscular blockade

Locations
Other Locations
Canada
University Health Network
RECRUITING
Toronto
Contact Information
Primary
Jenna Wong, MSc
jenna.wong@uhn.ca
4163404800
Time Frame
Start Date: 2020-10-01
Estimated Completion Date: 2027-03-01
Participants
Target number of participants: 23
Treatments
Experimental: Partial NMB
Sponsors
Leads: University Health Network, Toronto

This content was sourced from clinicaltrials.gov