A clinical trial to study the efficacy of different volumes of 0.2% ropivacaine in suprainguinal fascia iliaca compartment block for multimodal analgesia in lower limb surgery
Not Applicable
Not yet recruiting
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/09/036144
- Lead Sponsor
- Dayanand Medical College and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients scheduled for lower limb surgeries, including the hip and uptown the knee joint
-ASA I,II and III patients
-Cognitive ability to comprehend NRS scale
Exclusion Criteria
-Patient refusal
-Contraindications to the suprainguinal fascia iliaca compartment block (such as coagulopathies, infection at injection site, allergy to local anaesthetic)
-Patient on chronic opiod abuse
-Neuropathies
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To comparatively evaluate the efficacy of different volumes of ropivacaine in suprainguinal fascia iliaca compartment block for multimodal analgesia in lower limb surgeries <br/ ><br>-Time to first request of rescue analgesia with in first 24 hours after surgery <br/ ><br>-Total requirement of analgesics for pain management in first 24 hoursTimepoint: To comparatively evaluate the efficacy of different volumes of ropivacaine in suprainguinal fascia iliaca compartment block for multimodal analgesia in lower limb surgeries <br/ ><br>-Time to first request of rescue analgesia with in first 24 hours after surgery <br/ ><br>-Total requirement of analgesics for pain management in first 24 hours
- Secondary Outcome Measures
Name Time Method Patient satisfaction with pain managementTimepoint: 24 hours