Estimation of the minimum effective volume of 0.5% Levobupivacaine in ultrasound guided supraclavicular brachial block in patients undergoing upper limb orthopaedic surgeries.
Phase 2
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/08/045005
- Lead Sponsor
- Shimoga Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Patients aged 18-60 years and
2. Belonging to ASA physical status 1 or 2 and
3. Scheduled for forearm orthopaedic surgeries
Exclusion Criteria
1. Refusal of consent
2. Allergy to local anaesthetic
3. Pregnancy
4. Bleeding diathesis or coagulopathy
5. Contraindications absolute and relative to supraclavicular block
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method