A study to compare two different patches for pain relief after surgery of lower limb bone fracture
Not Applicable
Completed
- Conditions
- Health Condition 1: V899- Person injured in unspecified vehicle accident
- Registration Number
- CTRI/2019/02/017417
- Lead Sponsor
- Department of anaesthesiology Pt B D Sharma PGIMS Rohtak
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 75
Inclusion Criteria
Total no. of patients- 75
ASA- I to III
Patients undergoing surgery for proximal femoral fractures under spinal anesthesia
Exclusion Criteria
Patients having poly trauma with any other fracture, Obese, hepatic or renal impairment, myasthenia gravis, delirium tremens, skin allergy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual analogue scale (VAS) <br/ ><br> <br/ ><br>Post operative nausea and vomiting(PONV) <br/ ><br> <br/ ><br>Rescue analgesia <br/ ><br> <br/ ><br>ComplicationsTimepoint: Visual analogue scale (VAS) at 2 hrs,4 hrs,6 hrs,12 hrs,24 hrs,3rd day,5th day,7th day <br/ ><br> <br/ ><br>Post operative nausea and vomiting(PONV) at 2 hrs,4 hrs,6 hrs 12 hrs,24 hrs,3rd day, 5th day 7th day <br/ ><br> <br/ ><br>Rescue analgesia at 1st,2nd,3rd,4th,5th,6th,7th day <br/ ><br> <br/ ><br>Complications at 1st,2nd,3rd,4th,5th,6th,7th day
- Secondary Outcome Measures
Name Time Method Heart rate <br/ ><br> <br/ ><br>Mean arterial pressure <br/ ><br> <br/ ><br>SpO2Timepoint: Baseline, 15min, 30min, 1st hr, 2nd hr, 3rd hr, at the end of surgery