The effect of Ondansetron in combination with Apotel in pain control
Phase 3
- Conditions
- Patients with upper limb fractures..
- Registration Number
- IRCT2017062133566N1
- Lead Sponsor
- Vice chancellor for research, Golestan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
ASA Class 1; Upper limb fracture; Patients who undergo anesthesia with propofol as an anesthetic inducer; Satisfied to participate in the study; being at the age of 15 and older. Exclusion criteria: ASA grade 3 and 4; uncontrolled diabetes; history of ischemic heart disease (IHD); history of stroke; malignancy; psychiatric problems; Pregnancy; surgery duration greater than 120 minutes; history of substance abuse or drug abuse; Alcohol consumption; history of liver problems; history of Apotel (acetaminophen) sensitivity; history of nausea and vomiting after previous surgical procedure; Patients with long Q-T intervals.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: 24 hours and 48 hours after recovery. Method of measurement: Visual Analogue Scale.
- Secondary Outcome Measures
Name Time Method