A clinical trial to compare the analgesic effect of three modalities, epidural block , TAP block and combined parenteral diclofenac and tramodol in patients undergoing total abdominal hysterectomy.
Not Applicable
- Conditions
- Health Condition 1: null- quality of recovery in ASA I-II patients undergoing total abdominal hystercetomy
- Registration Number
- CTRI/2011/06/001823
- Lead Sponsor
- post graduate institute of medical education and research chandigarh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
1.ASA I-II patients
2.age 18-65 years
3.total abdominal hysterectomy +/- bilateral salpingo-oophorectomy
Exclusion Criteria
inability to cooperate
BMI >30
ASA grade > III(moderate to severe heart or lung disease)
history of drug or alcohol abuse
complaint of chronic pain/daily intake of analgesics
contraindications to NSAIDs/insertion of epidural catheter
undergoing omentectomy,lymph node dissection or radical hysterectomy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method quality of recovery as assessed by QOR-40Timepoint: postoperative at 24,48,72 hours
- Secondary Outcome Measures
Name Time Method postoperative pain scores as assessed by NRS and rescue analgesic(morphine) requirementTimepoint: postop at 0min,30 min, 60 min, 90 min, 2 hours, 4 hours ,6hours, 12 hours,18hours, 24hours