Clinical trial to study the comparison of ultrasound guided pericapsular nerve group block with or without clonidine.
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/08/072387
- Lead Sponsor
- Gopal krishan jalwal
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patient of either sex in the age group of 18 to 70 years with physical status ASA1 or ASA II
Exclusion Criteria
Consent refusal, Allergic history to local anaesthetic, abnormal coagulation profile, emergency surgeries, contraindications to regional anaesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Outcome TimePoints <br/ ><br>To evaluate the time to first analgesic request postoperatively.Timepoint: 24 hours
- Secondary Outcome Measures
Name Time Method 1)To calculate the Ease of spinal positioning score after performing the block for positioning of spinal anaesthesia <br/ ><br>2) To determine numerical rating scale pain scores at rest and at 15 degree leg elevation in both the groups <br/ ><br>3) To determine the total dose of analgesic requirement in the first 24 hours after surgery in both the patients groupTimepoint: 24 hours