Reduction of post-operative pain using intravenous acetaminophen, ketamine and tramadol in open renal surgeries
Phase 2
- Conditions
- post operation pain.Pelvic and perineal pain
- Registration Number
- IRCT201509143773N14
- Lead Sponsor
- Vice chancellor for research,Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Older than 18 years old; With ASA I & II. Exclusion criteria: patients with the history of opium use; history of psychological disorders; chronic low back pain.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: 5, 10, and 20 minutes after arriving to the recovery room, to the ward, and also 1 and 6 hours after transfer to the ward. Method of measurement: Visual Analog Scale.;Level of agitation. Timepoint: 5, 10, and 20 minutes after arriving to recovery room, time to transfer from recovery to the ward, and also 1 and 6 hours after transfer to the ward. Method of measurement: Richmond Sedation Scale.
- Secondary Outcome Measures
Name Time Method Opiom requirment. Timepoint: At recovery room and 6 hour after the surgery. Method of measurement: Submit file.;Patient hemodynamic. Timepoint: 5, 10, 20 minutes after the infusion and at exit the recovery room and 6 hour after the surgery. Method of measurement: Blood pressure and pulse rate (Monitoring instrument).