Actively Recruiting
Anesthesia Clinical Practice During Labour Neuraxial Analgesia
Led by University of British Columbia · Updated on 2025-07-24
19
Participants Needed
1
Research Sites
38 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this observational study is to evaluate the communication between the anesthesiologist and the patient prior the initiation and during the administration of the labor neuraxial analgesia. The investigators hypothesize that there will be differences among anesthesiologists during the informed consent process and communication during the procedure, specifically, how the anesthesiologists describe the technical aspects of the procedure, alternatives, risks, complications, and expected effects of labour neuraxial analgesia. The anesthesiologists will be observed during a routine labor neuraxial analgesia procedure for healthy uncomplicated patients.
CONDITIONS
Official Title
Anesthesia Clinical Practice During Labour Neuraxial Analgesia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- All obstetric anesthesiologists working in maternity unit
You will not qualify if you...
- Any comorbidity of the patient that would necessitate deviation from a routine practice for the initiation of labor neuraxial analgesia
AI-Screening
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Trial Site Locations
Total: 1 location
1
Department of Anesthesia at BC Women's Hospital, University of British Columbia.
Vancouver, British Columbia, Canada, V6H 3N1
Actively Recruiting
Research Team
V
Vit B Gunka, MD
CONTACT
J
Juliana Barrera, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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