Comparision of postoperative analgesia in patients undergoing hip surgeries with ultrasound guided fascia iliaca block using different local anaesthetics combination

Phase 4

Recruiting

• Conditions: Medical and Surgical,

• Registration Number: CTRI/2024/04/066191
• Lead Sponsor: Chamarajanagar Institute of Medical Sciences

Brief Summary

Most of the patients undergoing hip surgeries belong to geriatric age group and have multiple co morbidities and in whom providing effective analgesia is challenging. Since suprainguinal fascia iliaca compartment block is proposed to have prolonged analgesic effect and reduces the need of opiods which hasten the early mobilization, recovery and reduced hospital stay. Since there are a few studies on suprainguinal fascia iliaca compartment block the present study is being done to assess the efficacy in using adjuvants in suprainguinal fascia iliaca compartment block. The block is performed using ropivacaine 0.2% with adjuvants clonidine and dexmedetomidine to check for the efficacy of these drugs in prolongation of postoperative analgesia for hip surgeries.

Detailed Description

Not available

Study Timeline

• Study Start: 2024-09-05
• Last Update Posted: 2024-09-07

Recruitment & Eligibility

• Status: Open to Recruitment
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• Patient accepting to participate with written informed consent.
• Patients belonging to ASA with physical status grade 1 and 2 of either sex.
• Patient with age group between 18 to 70 years posted for elective major hip surgeries.

Exclusion Criteria

• Patient allergic to study drug or hypersensitivity to local anesthetics.
• Patient with cardiac disease, hepatic disease, renal disease, hypothyroidism, neuropathy, local site infection, bleeding diathesis, COPD, Obstructive sleep aponea .
• Patient on beta blockers, bradycardia (heart rate <60bpm).
• Patient with BMI >30 kg/m2.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain scores will be assessed as per visual analogue scale and the time needed for rescue analgesia	assessed over 24 hours every 5 minutes for first half an hour followed by every 2 hours for next 24 hours.

Secondary Outcome Measures

Name	Time	Method
a) To study hemodynamic changes between two groups of patients.	b) To assess the sedation among two groups of patients.

Trial Locations

Locations (1)

Chamarajanagar Institute of Medical Sciences Chamarajanaga; 🇮🇳 Chamarajanagar, KARNATAKA, India

Chamarajanagar Institute of Medical Sciences Chamarajanaga

🇮🇳Chamarajanagar, KARNATAKA, India

DR DARSHAN MS

Principal investigator

09741376797

darshanms_jss@yahoo.com