Determination of the effect of sedative of Dexmedetomidine and Fentanyl with Propofol and Fentanyl in participants undergoing colonoscopy
Phase 2
- Conditions
- Participants candidates for colonoscopy for diagnosis any disease.
- Registration Number
- IRCT20170805035510N4
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
ASA Class I, II
Exclusion Criteria
Patients with complete heart block
Liver failure
Severe heart failure
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sedation. Timepoint: After colonoscopy. Method of measurement: Visual Analogue Scale (VAS).
- Secondary Outcome Measures
Name Time Method Pain. Timepoint: After colonoscopy. Method of measurement: Visual Analogue Scale (VAS).