A clinical trial to compare the effects of 0.5% Ropivacaine with 1mL (0.3mg) Buprenorphine versus 0.5% Ropivacaine with 1mL Normal saline while giving Supraclavicular brachial plexus block for upper limb orthopaedic surgeries.
Phase 4
- Conditions
- Health Condition 1: O- Medical and SurgicalHealth Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2022/06/043277
- Lead Sponsor
- Mrigakshi Sarma
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. American Society of Anaesthesiology(ASA) physical status I and II.
2.Scheduled for elective Orthopaedic upper limb surgery under supraclavicular brachial plexus block.
3. Informed and written consent.
Exclusion Criteria
1.Unwilling patients.
2.Patients belonging to ASA physical status III or more.
3. Patients with known hypersensitivity to local anaesthetics.
4.Infection at the site of block.
5.Patients with known coagulopathy or patients on anticoagulation therapy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method