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A Trial Comparing Propofol to Midazolam Plus Meperidine Sedation for Outpatient Colonoscopy

NCT00848861 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 92

Last updated 2009-02-20

No results posted yet for this study

Summary

-to determine if propofol sedation leads to shorter recovery times compared to traditional sedation using midazolam plus meperidine

Conditions

  • Sedation

Interventions

DRUG

propofol (sedation for outpatient colonoscopy)

DRUG

midazolam plus meperidine (sedation for outpatient colonoscopy)

Sponsors & Collaborators

  • University of Alberta

    lead OTHER

Principal Investigators

  • Dina Kao, MD · University of Alberta

  • Eoin Lalor · University of Alberta

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-02-28
Primary Completion
2006-06-30
Completion
2006-06-30

Countries

  • Canada

Study Locations

More Related Trials

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 NCT00848861 on ClinicalTrials.gov