Compare the Efficacy of Ultrasound Guided Costoclavicular Block versus Supraclavicular Block for Shoulder Surgery
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/01/061071
- Lead Sponsor
- Sawai Mansingh Medical College and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Patients undergoing shoulder surgery.
2. Patients of either gender in age group of 20 to 60 years.
3. Patients of ASA grade I, II and III.
4. Patients with BMI of 18-30 kg/m2.
Exclusion Criteria
1. Patients not willing to participate in study and uncooperative patients.
2. Coagulopathies, any neuropathy.
3. Allergy to LA (Ropivacaine).
4. Local pathology at the injection site.
5. Disability limiting the performance of block
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.To assess and compare the nerve sparing in various dermatomes in both groups. <br/ ><br>2.To assess and compare the nerve sparing in both groups. <br/ ><br>3.To determine the difference in mean onset and mean duration of motor and sensory block in both groups. <br/ ><br> <br/ ><br>Timepoint: 1.Every 10 mins for 30 minutes after the block. <br/ ><br>2.Every 10 minutes for 30 minutes after the block. <br/ ><br>3.Every 10 minutes for 30 minutes after the block. <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1.To determine the difference in mean NRS score. <br/ ><br>2.To assess Hollmen grading of sensory block. <br/ ><br>Timepoint: 1.Every 10 minutes for 30 minutes after the block. <br/ ><br>2.At the end of 30 minutes after the block.