To evaluate the pain relief after combined femoral and sciatic nerve block for lower limb cancer surgeries
Not Applicable
- Conditions
- Health Condition 1: C00-D49- Neoplasms
- Registration Number
- CTRI/2024/03/064674
- Lead Sponsor
- Dr Viji S Pillai
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients undergoing lower limb onco surgeries with
Age between 15 and 60 years
ASA physical status 1,2 and 3
Exclusion Criteria
Patients with history of allergy to local anesthetics
Patients with history of bleeding disorders
Patients with spinal cord disorders and pre existing neurological deficits
Infection of the proposed site
Patients on long term opioid medication for pain relief
Refusal for regional procedure or to participate in study
BMI greater than 30
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Peri operative analgesic efficacy of combined femoral and sciatic nerve block assessed by numerical rating score for pain assessment at rest and at movementTimepoint: Post operative period intervals of 0, 6, 24 and 48 hours
- Secondary Outcome Measures
Name Time Method Intraoperative hemodynamic stability & additional opioid requirement during surgery. <br/ ><br>To observe the total requirement of rescue analgesia in 48 hours post operatively. <br/ ><br>To observe the time taken for ambulation post operatively. <br/ ><br>To comapare the above parameters with patients receiving epidural analgesia using historical dataTimepoint: Intra operative vitals will be recorded every 10 min. <br/ ><br>Post operatively patient evaluated at intervals of 0 6 24 & 48 hours