To determine the minimum volume of bupivacaine(which is a local anaesthetic)at which its effect can be achieved for USG guided supraclavicular brachial plexus block in surgeries related to arm, forearm, hand
Not Applicable
- Conditions
- Health Condition 1: S50-S59- Injuries to the elbow and forearmHealth Condition 2: S40-S49- Injuries to the shoulder and upper armHealth Condition 3: S60-S69- Injuries to the wrist, hand and fingers
- Registration Number
- CTRI/2023/09/057496
- Lead Sponsor
- I
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
After obtaining approval from institutional ethics committee and informed written consent will be taken from all 75 patients.
1. Patients of ASA grade - I , ASA grade II
2. Age group 18-60 years of either sex.
3. All patients scheduled for elective surgery posted for upper limb surgeries and requiring local anaesthesia
Exclusion Criteria
1. Patient refusal or not giving consent.
2. Pregnancy
3. Patient with comorbidities
4. Seizure disorder
5. ASA grade III, IV,V,E
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To find out the minimum volume of local anaesthetic bupivacaine(P) 0.5% for ultrasound guided supraclavicular brachial plexus nerve blockTimepoint: Sensory and motor block will be assessed till 120 min post block
- Secondary Outcome Measures
Name Time Method 1. To see duration of effect of bupivacaine(P) 0.5 %. <br/ ><br>2. To see adverse effect of drug, if any <br/ ><br>Timepoint: duration of block will be observed for next 24 hours side effects will be observed till 24 hours post block