Comparison of tourniquet pain between two types of brachial plexus block
Not Applicable
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/03/050667
- Lead Sponsor
- Department of Anesthesia, Pt BD Sharma PGIMS, Rohtak
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 44
Inclusion Criteria
ASA I to III, scheduled to undergo orthopaedic or plastic surgery distal to elbow with anticipated tourniquet duration greater than 45 minutes will be included
Exclusion Criteria
Patients with Contraindications to regional Anesthesia, local infection , distortion of local anatomy, allergy to local anaesthetics, chronic pain syndrome, clinically significant cognitive impairment, axillary clearance in past, pregnancy, history of peripheral neuropathy, refusal to give consent will be excluded.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method