To study the effect of FICB and PENG block under USG guidance for ease of positioning the patients for administrating spinal anaesthesia and post operative pain relief
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/06/043027
- Lead Sponsor
- Dr Santosh Kumar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients posted for fracture hip surgeries
Exclusion Criteria
Patient refusal.
Pregnancy and lactating mothers.
Altered coagulation profile or bleeding diasthesis.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual analogue scoring and numerical rating scale of pain of less than or equal to 3Timepoint: Visual analogue scoring and numerical rating scale of pain of less than or equal to 3 at 15 minutes, 30 minutes, one hour, 2 hour, 4th hour, 8th hour, 12th hour, 18th hour and 24th hour post surgery.
- Secondary Outcome Measures
Name Time Method To assess pain in visual analogue scoring and numerical rating scaleTimepoint: Post-operative for 24 hours