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Clinical Trials in Canada / NCT07083167
Recruiting Observational

Anesthesia Clinical Practice During Labour Neuraxial Analgesia

NCT07083167 · tracked via the Priya Life Science Canada tracker
Phase
Observational
Started
2025-04-02
Last updated
2025-07-24

Condition(s) studied

Labor Analgesia

Investigational drug(s) / intervention(s)

No Interventions.

No Interventions.: No interventions.

Study summary

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.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * all obstetric anesthesiologists working in maternity unit Exclusion Criteria: * any comorbidity of the patient that would necessitate deviation from a routine practice for the initiation of labor neuraxial analgesia

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Department of Anesthesia at BC Women's Hospital, University of British Columbia. Vancouver British Columbia Recruiting

More University of British Columbia trials in Canada

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07083167 on ClinicalTrials.gov ↗ ← All trials in Canada