Comparing two different types of upper limb blocks in clavicle surgeries
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/02/063293
- Lead Sponsor
- Dr Shivakumar G
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
BMI of 18.5 to 24.9 kg per sq meter
Patients undergoing clavicle surgeries with either SCUT block or interscalene block
ASA PS grades I and II
Patients ready to give informed consent
Exclusion Criteria
Patients with opioid drug intake for other conditions
Patients on any routine analgesics
Patients who are known diabetics
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome which is measured is maximum time of post operative analgesia after giving block.Timepoint: 24hours
- Secondary Outcome Measures
Name Time Method To compare onset and regression of sensory and motor blockade between the groups after giving blockTimepoint: 24 hours