Sedative effect of ketamine with propofol in colonoscopy

Phase 3

Recruiting

• Conditions: Colonoscopy.; Failed moderate sedation during procedure; T88.52

• Registration Number: IRCT20220706055402N3
• Lead Sponsor: Ahvaz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 13 March 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 120

Inclusion Criteria

Age range of 18 to 65 years old
Patient willingness to participate in the study
Patients who are in the American Society of Anesthesiology class 1 and 2.

Exclusion Criteria

The patient's unwillingness to participate in the study
Intestinal perforation during the procedure
Esophageal or stomach or intestinal bleeding during the procedure
Changing the type of procedure during colonoscopy or the need for surgery during the procedure

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
evel of sedation. Timepoint: From start to end of colonoscopy. Method of measurement: Ramsay Sedation Scale.;Amount of pain. Timepoint: From start to one hour after colonoscopy. Method of measurement: Visual Analogue Scale.