A clinical study to compare effectiveness and safety between blocks given to neck region for upper arm surgeries using ultrasound guidance and peripheral nerve stimulator needle guidance.
Phase 2
- Conditions
- Health Condition 1: M958- Other specified acquired deformities of musculoskeletal systemHealth Condition 2: M844- Pathological fracture, not elsewhere classified
- Registration Number
- CTRI/2024/01/061827
- Lead Sponsor
- Mysore medical college and research institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Adult patients of either sex , aged between 18- 55 years belonging to ASA class 1 and class 2 without any severe comorbid diseases scheduled for elective upper arm surgeries
Exclusion Criteria
Age less then 18 years and more than 55 years
ASA class 3 , 4 , 5
Cardiovascular , respiratory an neurological disorders and myopathies
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To asses procedural time, onset of sensory and motor block, number of inadvertent vascular punctures between ultrasound guided and peripheral nerve stimulator method Interscalene brachial plexus block in upper arm surgeriesTimepoint: 30min
- Secondary Outcome Measures
Name Time Method To find out hemodynamic parameters; heart rate, systolic blood pressure, diastolic blood pressure, mean arterial pressure at various intervals following Interscalene brachial plexus comparing ultrasound guided and peripheral nerve stimulator methodsTimepoint: 3 hours