Randomised controlled trial of patient controlled sedation for colonoscopy: entonox vs target controlled infusion of propofol

Completed

• Conditions: Surgery: Analgesia; Surgery; Analgesia

• Registration Number: ISRCTN65879800
• Lead Sponsor: Record Provided by the NHSTCT Register - 2007 Update - Department of Health

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2007-09-28
• Last Update Posted: 13 January 2015

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

All patients of both sexes undergoing elective colonoscopy will be recruited.

Exclusion Criteria

Patients with chronic pulmonary disease, history of colonic resection, intolerance to any of the drugs, unwilling to enter trial, ASA class IV, allergy to soybeans, eggs, history of seizure disorder, sleep apnoea, or difficult intubation, a short thin neck or the inability to open mouth widely.

Study & Design

• Study Type: Interventional
• Study Design: Not specified