Comparing two different methods Of reducing pain in patients with bone issues undergoing operations requiring taking Of part of bone from the hip area
Phase 3
- Conditions
- Health Condition 1: 8- Other Procedures
- Registration Number
- CTRI/2024/05/067488
- Lead Sponsor
- Institutional Fluid Grant
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA class 1,2,3
Exclusion Criteria
age less than 18years, ASA 4, Deranged coagulation profile, peripheral neuropathy, local anaesthetic allergy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the post operative pain by VAS scores in the two groups at rest and movementTimepoint: To assess the post operative pain by Visual analog scale scores in the two groups at rest and movement at 6,12,24,36,48,60,72hrs post surgery after the intervention
- Secondary Outcome Measures
Name Time Method eed for rescue analgesia and functional outcome based on early ambulationTimepoint: at 6,12,24,36,48,60,72 hours post surgery