A Study To Evaluate The Change In Perfusion Index As An Indicator Of Successful Ultrasound Guided Supraclavicular Block
Not Applicable
- Conditions
- Health Condition 1: M00-M99- Diseases of the musculoskeletal system and connective tissueHealth Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2023/09/057849
- Lead Sponsor
- ELMCH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients undergoing elective surgeries of the upper limb (wrist, hand, forearm) ASA physical status I & II
Exclusion Criteria
Patients with allergy to local anaesthetics and study drugs, Who have local pathology at the site of injection, Pre existing peripheral neuropathy of the upper limb, Suspected brachial plexus injury, History of any systemic disease (HTN, DM), convulsion or bleeding disorder
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Perfusion Index can be used as a simple and objective tool to predict a successful ultrasound guided supraclavicular block in patients undergoing upper limb surgeries.Timepoint: intraoperatively- 0 mins, 2 mins, 4mins, 6 mins, 8 mins, 10mins, 15 mins, 20mins, 25 mins, 30mins
- Secondary Outcome Measures
Name Time Method Perfusion Index can be used as a simple & objective tool to predict a successful ultrasound guided supraclavicular block in patients undergoing upper limb surgeries.Timepoint: perfusion index will be recorded at baseline, 2 mins, 4 mins, 6 mins, 8 mins, 10 mins, 15 mins, 20 mins, 25 mins, 30 mmins interval after the block