A clinical study to compare the paralysis of diaphragm after giving regional anesthesia for upper limb surgeries via different approaches
Phase 2
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/04/065368
- Lead Sponsor
- Dr Sayantanee Roy
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Age 18-60 years
ASA 1 and 2
Scheduled for elective orthopaedic upper limb surgery under supraclavicular brachial plexus block and costoclavicular brachial plexus block
Informed and written consent to participate in the study
Exclusion Criteria
Patients with known hypersensitivity to local anaesthetic agent
Infection at the site of block
Patient with known respiratory disorder
Patient whose pre operative SpO2 is less than 95%
Patients with known coagulopathy or on anti-coagulation therapy
Patients with diabetes mellitus
Pregnant and lactating mother
Morbid obesity
Patients on chronic analgesic therapy
Patients with peripheral vascular disease
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. To compare the incidence of hemi diaphragmatic paralysis with supraclavicular and costoclavicular brachial plexus approach <br/ ><br> <br/ ><br>Timepoint: Outcome will be assessed at 30 minutes after giving the block in the two groups .
- Secondary Outcome Measures
Name Time Method 1.To compare the extent of diaphragmatic excursion between both groups <br/ ><br>2. To check for side effects and complications <br/ ><br>3.To compare the onset of block between two groups <br/ ><br>4.To compare the duration of analgesia between two groups. <br/ ><br>Timepoint: Outcome will be assessed at the following time intervals at rest : <br/ ><br>0 hour , 3 minutes ,15 minutes ,30 minutes.