Comparative study of bupivacaine and levobupivacaine with adjuvant buprenorphine in brachial plexus block in upper limb surgeries
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/02/063071
- Lead Sponsor
- JSS Academy of Higher Education and Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Age between 18 years-60 years
- ASA-PS I and II
- Posted for upper limb surgeries
Exclusion Criteria
-Patient not giving consent
-Coagulopathy
-Neuropathy
-Pregnancy
-Hemodynamic instability
-Allergic history to local anesthetic
-Local infection, open wound , distorted anatomy in the affected side of neck and supraclavicular area due to hematoma, swelling
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the effect of block and duration of analgesia by adding adjuvant buprenorphine to bupivacaine and levobupivacaineTimepoint: From giving supraclavicular brachial plexus block to 24 hours postoperative period
- Secondary Outcome Measures
Name Time Method To determine onset and duration of sensory block using Holmen scale, to determine onset and duration of motor block using modified bromage scale, to determine total duration of postoperative analgesia using VAS score, any side effects like nausea, vomiting, pruritis, respiratory depressionTimepoint: From giving supraclavicular brachial plexus block to 24 hours postoperative period