Comparison effect of Propofol-Fentanyl with Propofol-Ketamine for sedation in patients undergoing ERCP
Not Applicable
- Conditions
- (Endoscopic Retrograde Cholangio Pancreatography)ERCP.Fluoroscopy of Biliary and Pancreatic Ducts using Low Osmolar Contrast
- Registration Number
- IRCT2014031316976N1
- Lead Sponsor
- Vice chancellor for research, Ahvaz Jundishapur University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 98
Inclusion Criteria
admitted patients for diagnostic and therapeutic ERCP in Imam Khomeini hospital; 18 to 65 years old; anesthesia risk of 1, 2 (According to American society of anesthesiologist's classification).
Exclusion criteria: patient refuse; under 18 and over 65 years old; a history of drug abuse; sensitivity to egg; contraindication of Fentanyl or Ketamine.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sedation Score. Timepoint: Four times, during procedure. Method of measurement: Ramsay Sedation Score.
- Secondary Outcome Measures
Name Time Method Pain. Timepoint: One hour after procedure. Method of measurement: Visual Analogue Scale.;Nausea. Timepoint: One hour after procedure. Method of measurement: Zero for not having nausea, One for mild nausea, Two for moderate nausea and Three for sever nausea.;Vomiting. Timepoint: One hour after procedure. Method of measurement: Zero for the patients not experiencing vomiting, 1 for the little vomiting, 2 for vomiting gastric contents and 3 for vomiting food particles.