Comparison of Etomidate-Fentanyl and Propofol -Fentanyl sedation in patients scheduled for colonoscopy
Not Applicable
- Conditions
- Patients with intestine diseases who need colonoscopy.disease of intestine,unspecified
- Registration Number
- IRCT201212195381N4
- Lead Sponsor
- Vice-chancellor of Research Babol University Of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Male
- Target Recruitment
- 80
Inclusion Criteria
patients scheduled for comlete elective colonoscopy;ages of 18-55 years;ASA 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.
Exclusion Criteria
Not provided
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.