Comparison of sedative and analgesic effects of two combinations of dexmethomidine-ketamine (Ketodex) and propofol-fentanyl (Fenofol)
Phase 3
Recruiting
- Conditions
- Analgesia and sedation in patients undergoing endoscopic retrograde cholangiopancreatography.
- Registration Number
- IRCT20160307026950N55
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
Age over 18 years
Consent to enter the study
Patients who are candidates for endoscopic retrograde cholangiopancreatography
Patients with American Society of Anesthesiologists (ASA) I,II
Exclusion Criteria
Patients with high blood pressure, coronary heart disease and central nervous system disorders
Patients with known allergies to study drugs
pregnancy
Airway's disease
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sedation rate of patients. Timepoint: The base time (before the start of the intervention) and then every 15 minutes in the operating room and in the first hour of recovery every 15 minutes to 45 minutes and then in the 2nd and 4th hours after ERCP were recorded. Method of measurement: The level of patients sedation will be evaluated using the Modified Aldrete score,whose validity and reliability have been confirmed by a recent stud.;Analgesia of patients. Timepoint: The base time (before the start of the intervention) and then every 15 minutes in the operating room and in the first hour of recovery every 15 minutes to 45 minutes and then in the 2nd and 4th hours after ERCP were recorded. Method of measurement: Painlessness of patients will be evaluated using the Visual Analogue Scale (VAS) whose validity and reliability have been confirmed by a recent study.
- Secondary Outcome Measures
Name Time Method