TO See occurrence of diaphragmatic paralysis in patients after recieving Supraclavicular v/s Costoclavicular brachial plexus block in upper limb surgeries
Phase 3
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/10/058697
- Lead Sponsor
- SMS Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
patients posted for upperlimb surgeries
ASA grade 1-2
weight 40-90kgs
Exclusion Criteria
patients not willing to participate
rib fracture , icd for pneumothorax , allergic to local anaesthetics
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.To determine the difference in mean height of hemidiaphragm before, 30 and 60 mins after block in patients using Ultrasonography <br/ ><br>to determine difference in MEAN PEFR <br/ ><br>Timepoint: 1.To determine the difference in mean height of hemidiaphragm before, 30 and 60 mins after block in patients using Ultrasonography <br/ ><br>to determine difference in MEAN PEFR <br/ ><br>
- Secondary Outcome Measures
Name Time Method Difference in mean PEFR is calculatedTimepoint: 0mins ,30 mins , 60 mins