Status:
COMPLETED
A Study to Examine Levels of Sedation During Outpatient Colonoscopies
Lead Sponsor:
Baylor Research Institute
Conditions:
Outpatient Colonoscopy
Eligibility:
All Genders
18+ years
Brief Summary
Examine levels of sedation required for patients to comfortably undergo colonoscopy using propofol and if adjunct monitoring equipment promotes patient safety.
Detailed Description
Propofol for sedation during outpatient endoscopy has become a popular technique in place of midazolam and opioid sedation. It has been associated with improved patient satisfaction and a faster recov...
Eligibility Criteria
Inclusion
- Greater than 18 years of age
- ASA classification of I, II, or III
Exclusion
- Anesthesiologist plans to use a combination of medications other than propofol for sedation.
- ASA classification IV or higher
- Lesions on forehead or earlobes
Key Trial Info
Start Date :
March 1 2006
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
December 1 2006
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT00614263
Start Date
March 1 2006
End Date
December 1 2006
Last Update
June 12 2017
Active Locations (1)
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1
Baylor University Medical Center - Department of Anesthesiology
Dallas, Texas, United States, 75246