To reduce pain in fracture patients by giving local nerve block vs intravenous opiod
Phase 2
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/01/061719
- Lead Sponsor
- All India Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Adult of both gender from eighteen to eighty years presenting to emergency department with history of trauma and triaged as yellow or green and having upper or lower limb fractures with on arrival pain score greater than or equal to seven and patient or legally authorized representative gives consent
Exclusion Criteria
Patient or legally authorized representative is unable or unwilling to give consent or red triaged patients or patients with unstable vitals on arrival or less than eighteen years or greater than eighty years or patients with life threatening comorbidities or history of hypersensitivity or known contraindication to local anaesthetics or pain score less than seven
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To study and compare the pain score reduction during initial six hours of interventionTimepoint: 1hour,3hour,6hour
- Secondary Outcome Measures
Name Time Method To study complications of block procedure & compare with complications of opiod usageTimepoint: Over 6 hours;To study the length of emergency department stayTimepoint: In hours;To study the reduction in opiod usage due to block procedureTimepoint: Over 6 hours;To study the time taken to do the procedureTimepoint: In minutes;To study the time taken to reduce the pain after interventionTimepoint: In minutes