A Study to Examine Levels of Sedation During Outpatient Colonoscopies

NCT00614263 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2017-06-12

No results posted yet for this study

Summary

Examine levels of sedation required for patients to comfortably undergo colonoscopy using propofol and if adjunct monitoring equipment promotes patient safety.

Conditions

  • Outpatient Colonoscopy

Sponsors & Collaborators

  • Baylor Research Institute

    lead OTHER

Principal Investigators

  • Michael Ramsay, MD · Baylor Research Institute

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-03-31
Primary Completion
2006-12-31
Completion
2006-12-31

Countries

  • United States

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 NCT00614263 on ClinicalTrials.gov