Thigh block for post operative pain management after total hip arthroplasty operatio
Not Applicable
- Conditions
- Health Condition 1: V00-Y99- External causes of morbidity
- Registration Number
- CTRI/2020/06/025903
- Lead Sponsor
- il
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA 1 and 2,
Patient willing to participate
Patients with indication for THR
Exclusion Criteria
ASA 3 and 4
Patients refusing to participate
Pregnant woman
Patients having allergy to local anaesthetics
Failed subarachnoid block
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the efficacy of the FICB after hip arthroplasty surgery for pain relief during the post operative periodTimepoint: The pain scores will be assessed in 6,8,12hours post surgery
- Secondary Outcome Measures
Name Time Method To evaluate for early rehabilitation following hip arthroplasty surgeriesTimepoint: Post operative and follow-up upto 3 weeks post surgery