comparing the effectiveness of a drug with and without additives in post-operative pain relief among patients undergoing hip and lowerlimb surgeries
Not Applicable
- Conditions
- Health Condition 1: M968- Other intraoperative and postprocedural complications and disorders of musculoskeletal system, not elsewhere classifiedHealth Condition 2: M970- Periprosthetic fracture around internal prosthetic hip joint
- Registration Number
- CTRI/2024/02/062313
- Lead Sponsor
- Saveetha medical college and hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)Patients undergoing Dynamic hip screw fixation, Total hip replacement & Proximal femoral nailing
2)ASA I & II patients
Exclusion Criteria
1)Patient refusal
2)Critically ill patients (ASA III & above)
3)Evidence of coagulopathy
4)Infection at the site of puncture
5)Pregnant patients
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The duration of post-operative analgesia between 0.25% ropivacaine, ropivacaine with dexmedetomidine, and ropivacaine with dexamethasone will be assessed and compared using VAS score post operatively <br/ ><br> <br/ ><br>Timepoint: VAS score during the post-operative period at 2 hours,6 hours,12 hours,24 hours.
- Secondary Outcome Measures
Name Time Method The time of requirement of rescue analgesia between the three groups will be assessed & comparedTimepoint: Time of rescue analgesia in hours assessed at 2hours, 6 hours, 12 hours & 24 hours post operatively