A Randomised controlled trial of infraclavicular versus costoclavicular approach of Infraclavicular block in upper limb surgery
Not Applicable
Not yet recruiting
- Conditions
- Health Condition 1: M849- Disorder of continuity of bone, unspecified
- Registration Number
- CTRI/2021/08/035491
- Lead Sponsor
- ady hardinge medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All patients >18yrs of ASA1 and 2 of either sex.
Exclusion Criteria
1.Upper limb surgeries above mid humerus level.
2. Any known drug allergies.
3.Contraindication to nerve block like coagulopathy, bleeding diathesis and local infections.
4.Preexisting neurological deficit.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Mean opioid consumption(mg/kg) at the end of 24 hours poatoperatively in both paracoracoid and costoclavicular infraclavicular block groups.Timepoint: Mean opioid consumption(mg/kg) at the end of 24 hours poatoperatively in both paracoracoid and costoclavicular infraclavicular block groups.
- Secondary Outcome Measures
Name Time Method 1. To compare the Pain score (Numerical Rating Scale (NRS)) on rest at 0,6,12 and24 hours postoperatively in both groups. <br/ ><br>2. To compare the Pain score (NRS) on limb movement at 0,6,12 and 24 hours postoperatively in both groups. <br/ ><br>3. To assess any catheter related complications (catheter dislodgement, erythema, hematoma at the site of catheter insertion) in both groups.Timepoint: 0,6,12 and 24 hours postoperatively