Comparison of sedative effect of propofol_ketamine and propofol_fentanyl in endoscopy procedure
Phase 3
Recruiting
- Conditions
- Sedation in patients undergoing endoscopy.
- Registration Number
- IRCT20200920048770N1
- Lead Sponsor
- Ahvaz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 86
Inclusion Criteria
All patients aged 18 to 65 years who have referred to Imam Khomeini Hospital in Ahvaz for endoscopic procedure
Exclusion Criteria
Patients under 18 or over 65 years of age
The patient's unwillingness to participate in the study
Patients contraindicated in propofol ketamine or propofol fentanyl
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sedation. Timepoint: Before and during the intervention. Method of measurement: Ramsay sedation scale.
- Secondary Outcome Measures
Name Time Method Pain. Timepoint: Before and during the intervention. Method of measurement: Ambesh scor.;Nausea. Timepoint: After the end of the intervention until the exit from recovery. Method of measurement: According to the visual analog scale ( vas )on a ruler that is scaled from zero to ten, zero is equivalent to nausea and ten is equivalent to maximum nausea.;Vomiting. Timepoint: After the end of the intervention until the exit from recovery. Method of measurement: Count the number of vomits.