Comparison of pain levels after abdominal surgery in patients receiving pregabalin and famotidine with pregabalin and diphenhydramine
Phase 2
- Conditions
- Abdominal surgery.
- Registration Number
- IRCT20230106057067N1
- Lead Sponsor
- Islamic Azad University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 34
Inclusion Criteria
Age 15-75 years old
Informed and written consent
ASA class 1 or 2
No abuse of drugs and alcohol
Elective surgery
Exclusion Criteria
Loss of consciousness
Hemodynamic disorder
Abnormal intraoperative bleeding
Operation is more than 4 hours
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method PAIN. Timepoint: After entering recovery and 24, 12, 6 hours after the operation. Method of measurement: Visual Analog Scale.
- Secondary Outcome Measures
Name Time Method