Comparison of the effects and side effects of sedation with propofol protocol and midazolam and pethidine protocol in endoscopic patients.
Phase 4
Recruiting
- Conditions
- Condition 1: Endoscopy under sedation by propofol. Condition 2: Endoscopy under sedation with midazolam and pethidine.-
- Registration Number
- IRCT2017070834959N1
- Lead Sponsor
- Vice-Chancellor for Research Affairs of Ahvaz Jundishapur University of Medical Sciences.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 266
Inclusion Criteria
Age above 18y/o; Consciousness; Ability to participate in the gastrointestinal tract endoscopy under sedation.
Exclusion criteria: Non-consciousness; allergy to anesthetic drugs.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of the endoscopy. Timepoint: GI endoscopy—from start to finish. Method of measurement: Stopwatch.;Recovery time after endoscopy. Timepoint: After endoscopy. Method of measurement: Stopwatch.;Patient satisfaction after endoscopy. Timepoint: After endoscopy. Method of measurement: Score expressed by the patient.
- Secondary Outcome Measures
Name Time Method Hypoxia. Timepoint: Before intervention and after intervention. Method of measurement: Pulse oximetry.;Cardiac arrhythmia. Timepoint: Before intervention and after intervention. Method of measurement: Heart monitoring.;Blood pressure. Timepoint: Before and after intervention. Method of measurement: Sphygmomanometer.;Nausea. Timepoint: ?After intervention. Method of measurement: Observation.;Vomiting. Timepoint: ?After intervention. Method of measurement: Observation.