Your session is about to expire
← Back to Search
Study trial for Pulmonary Hemorrhage (BloodyBlocker Trial)
N/A
Waitlist Available
Led By F Robert Purdy, FRCA
Research Sponsored by University of British Columbia
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up within 10 minutes from successful intubation
Awards & highlights
BloodyBlocker Trial Summary
This trial will compare a new bronchial blocker device against 3 existing methods of lung isolation in an emergency scenario.
Eligible Conditions
- Pulmonary Hemorrhage
BloodyBlocker Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ within 10 minutes from start of direct laryngoscopy
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~within 10 minutes from start of direct laryngoscopy
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Total time to successful lung isolation.
Secondary outcome measures
Model utility
Time to successful intubation
Time to successful method placement
BloodyBlocker Trial Design
1Treatment groups
Experimental Treatment
Group I: Study trialExperimental Treatment1 Intervention
All participants will perform pulmonary blockade on an intubating manikin using 4 different methods: Endobronchial intubation with an endotracheal tube; Bronchial blocker attached to the outside of an endotracheal tube; Double lumen endotracheal tube; and Intraluminal placement of bronchial blocker.
Find a Location
Who is running the clinical trial?
University of British ColumbiaLead Sponsor
1,415 Previous Clinical Trials
2,466,996 Total Patients Enrolled
F Robert Purdy, FRCAPrincipal InvestigatorThe University of British Columbia
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Share this study with friends
Copy Link
Messenger