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Anesthesia Clinical Practice During Labour Neuraxial Analgesia

NCT07083167 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 19

Last updated 2025-07-24

No results posted yet for this 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.

Conditions

  • Labor Analgesia

Interventions

OTHER

No Interventions.

No interventions.

Sponsors & Collaborators

  • University of British Columbia

    lead OTHER

Principal Investigators

  • Vit B Gunka, MD · Department of Anesthesia at BC Women's Hospital

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-04-02
Primary Completion
2025-09-30
Completion
2025-12-30

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07083167 on ClinicalTrials.gov