Effect of propofol-ketamin and propofol-fentanyl in colonoscopy

Phase 2

• Conditions: disease of intestine,unspecified.; disease of intestine,unspecified; k63.9

• Registration Number: IRCT20190529043750N1
• Lead Sponsor: Babol University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 26 August 2019

Recruitment & Eligibility

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

Inclusion Criteria

patients scheduled for comlete elective colonoscopy
18-55 years old
ASA class I-II

Exclusion Criteria

History of large bowel surgery
Pregnancy
Patients with psychiatric and emotional disorder
History of addiction
History of allergic reaction
History of pulmonary and metabolic disorders

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Before of discharge. Method of measurement: Visual Analogues Scale.

Secondary Outcome Measures

Name	Time	Method
Drug adverse effects. Timepoint: Before and after colonoscopy. Method of measurement: Before and after colonoscopy.;Colonoscopist satisfaction. Timepoint: After colonoscopy. Method of measurement: Numerical rating scale for colonoscopist satisfaction.;Blood pressure. Timepoint: Every 5 minutes. Method of measurement: Noninvasive cuff measurrment.;Heart rate. Timepoint: Every 5 minutes. Method of measurement: Pulse counting.