The effect of propofol or propofol plus midazolam and/or fentanyl on cognitive impairment following colonoscopy

Phase 4

Completed

• Conditions: Patients undergoing colonoscopy; Other - Normal oral and gastrointestinal development and function

• Registration Number: ACTRN12606000503527
• Lead Sponsor: Melbourne Health Research Directorate

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2006-12-05
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 200

Inclusion Criteria

Patients who present for elective outpatient colonoscopy, not combined with other procedures and following full bowel preparation.

Exclusion Criteria

Patients with cognitive deficits and without adequate English language comprehension.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Cognitive impairment[At discharge from colonoscopy suite]

Secondary Outcome Measures

Name	Time	Method
1. Depth of sedation every 5 min during sedation[Every 5 min while patients are sedated during colonoscopy.];2. Endoscopist satisfaction with intraoperative conditions[Measured at the end of colonoscopy];3. Complications[Recorded at the end of colonoscopy];4. Dreaming during sedation [Recorded on emergence from sedation]