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Conscious Sedation Versus Anesthesia for ERCP

NCT05220774 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 3174

Last updated 2024-01-09

No results posted yet for this study

Summary

Studies directly comparing EDCS with AAS during ERCP are scarce, varying widely in their designs and reaching conflicting conclusions regarding safety and effectiveness. The investigators will assess, via a multi-center prospective study, the success, adverse event rates, and patient tolerability of ERCP when performed under AAS versus EDCS.

Conditions

  • ERCP

Sponsors & Collaborators

  • McGill University

    collaborator OTHER

  • University of Ottawa

    collaborator OTHER

  • Queen's University

    collaborator OTHER

  • Halton Health (Oakville)

    collaborator UNKNOWN

  • Island Health, Victoria, BC

    collaborator OTHER

  • Radboud Medical Center

    collaborator UNKNOWN

  • University of Calgary

    lead OTHER

Principal Investigators

  • Nauzer Forbes, MD, MSc · University of Calgary

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-10-01
Primary Completion
2023-08-30
Completion
2023-11-30

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 NCT05220774 on ClinicalTrials.gov