The effect of combination of dexmedetomidine-bupivacaine with ketamine-bupivacaine on post poerative pain after lower abdominal surgeries
Phase 3
Recruiting
- Conditions
- anesthesia.
- Registration Number
- IRCT20090129001615N9
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
atients who are candidates for elective lower abdominal surgery
Age range 18-65 years
ASA 1 or 2
Exclusion Criteria
Patients with a history of allergy to the studied drugs (dexmedetomidine, ropivacaine, and ketamine)
Patients with a history of drug addiction
Patients with mental health problems
Obese patients weighing more than 100 kg
Patients with inability to express pain intensity based on VAS criteria
Infection at the surgical incision site
Any change in anesthesia method
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Post operatie pane. Timepoint: Every 15 minutes during recovery and at 2, 6, 12 and 24 hours after the operation. Method of measurement: With using vigual analog scale.
- Secondary Outcome Measures
Name Time Method