Assessment of the prophylactic combined effect of diphenhydramine with paracetamol on agitation and pain after laparoscopic cholecystectomy
Phase 3
Recruiting
- Conditions
- Cholecystectomy.
- Registration Number
- IRCT20170411033365N4
- Lead Sponsor
- Oroumia University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Age group 20 to 60 years
Patients with ASA class one and two undergo laparoscopic cholecystectomy
Selective general anesthesia
Exclusion Criteria
Patients aged 20 to 60 years with ASA class one and two undergoing laparoscopic cholecystectomy
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Agitation and pain. Timepoint: In recovery and after transfer to the ward at 6, 12 and 24 hours after surgery. Method of measurement: The amount of visual scoring pain (VAS) from zero to 10 points and the amount of agitation at the time of recovery after 10, 20, 30 minutes after recovery, by four-point scale.
- Secondary Outcome Measures
Name Time Method