Comparison of the efficacy of erector spinae block using bupivacaine versus ropivacaine for post operative pain relief
Phase 3
- Conditions
- Health Condition 1: K00-K95- Diseases of the digestive system
- Registration Number
- CTRI/2019/05/018955
- Lead Sponsor
- Bangalore Medical College and Research Institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients who gave written informed consent.
-Patients undergoing laparoscopic surgery under general anaesthesia.
-Patients belonging to ASA I and II.
Exclusion Criteria
-Patients who refused to give written informed consent for Erector spinae block.
-Hypersensitivity to the drugs used.
-Patients with systemic illness such as uncontrolled diabetes mellitus, neuromuscular disorder.
-Patients with bleeding diathesis.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of Analgesia based on pilot studiesTimepoint: 60 minutes
- Secondary Outcome Measures
Name Time Method VAS score and 24 hour analgesic requirement <br/ ><br>Timepoint: 24 hour