Propofol sedation during diagnostic colonoscopy

Completed

• Conditions: Patients undergoing a colonoscopy; Not Applicable

• Registration Number: ISRCTN51098340
• Lead Sponsor: Institutional Ethics Committee of the Clinical Center of Serbia

Brief Summary

2016 results in: https://www.ncbi.nlm.nih.gov/pubmed/29653037

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2014-10-25
• Study Start: 2015-09-14
• Last Update Posted: 28 May 2018

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 90

Inclusion Criteria

1. Aged between 18 and 65 years old
2. Body weight from 50 to 120 kg
3. Classified to groups I (normal, healthy patient) or II (mild systemic disease) according to the American Society of Anesthesiologists
4. Scheduled for diagnostic outpatient colonoscopy with deep sedation

Exclusion Criteria

1. Allergy to the study drugs
2. Previous problems with anesthesia or sedation
3. History of stridor snoring or sleep apnea
4. Neck abnormalites
5. Those classified to groups III or IV of Mallampati classification.

Study & Design

• Study Type: Interventional
• Study Design: Not specified