Comparison of the pain relief with the addition of clonidine along with bupivacaine in ultrasound-guided rectus sheath block in patients undergoing midline incisional hernia repair
Phase 4
Completed
- Conditions
- Health Condition 1: - Health Condition 2: - Health Condition 3: - Health Condition 4: K429- Umbilical hernia without obstruction or gangrene
- Registration Number
- CTRI/2019/02/017496
- Lead Sponsor
- niversity College of Medical Sciences and GTB Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
•Patients of ASA class I or II undergoing midline incisional hernia repair under general anaesthesia
Exclusion Criteria
Morbid obesity (BMI>= 35kg/m2)
Significant cardiac, hepatic or renal disease
Local infection at site of block
Pre-existing coagulation disorder
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The Time to first request of analgesiaTimepoint: The Time to first request of analgesia
- Secondary Outcome Measures
Name Time Method â?¢VAS scoreTimepoint: at every 30 minutes for 2 hours at the end of 4th, 6th, 12th, and 24th hours;Total tramadol consumptionTimepoint: At the end of 24 hours