Comparative study between two block technique that helps in pain management of hip fracture patients

Not yet recruiting

• Conditions: Fracture of head and neck of femur,

• Registration Number: CTRI/2020/11/029247
• Lead Sponsor: ALL INDIA ISTITUTE OF MEDICAL SCIENCES NEW DELHI

Brief Summary

The study is a randomized controlled trial-a pilot study to **compare analgesic efiicay between pericapsular nerve group block and fascia iliaca block for positioning in hip fracture patients before neuraxial block** using VAS score,sitting angle, anaesthetist satisfaction, patient satisfaction, 24 hour toatal analgesic cosumption. The drug used is 20ml 0.25% ropivacaine in each group,and procedure will be ultrasound guided.There is no comparitive study between these two block ,hence investigator proposed this trial

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2020-11-18
• Study Start: 2020-11-30

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

Patients with age above 18 years, undergoing surgery for hip fracture under neuraxial block.

Exclusion Criteria

• Patient refusal.
• Any contraindication to neuraxial block like coagulopathy, local infection, increased ICP, spine trauma etc.
• Known allergy to local anaesthetic drugs.
• Peripheral neuropathy.
• Hemodynamically unstable polytrauma patients.
• Patients who are ASA 4 and above.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To assess and compare the analgesic efficacy of USG guided pericapsular nerve group (PENG) block with fascia iliaca compartment block (FICB) using VAS score during positioning of hip fracture patients within 30 minutes before neuraxial block.	At 10, 20, 30 minutes

Secondary Outcome Measures

Name	Time	Method
To compare the quality of positioning in the two groups for neuraxial block which will be assessed by the anaesthesiologist’s satisfaction and spinal angle.	At 30 minute
To compare the patient’s acceptance of the technique.	At 24 hour
To study any complications associated with the block.	24 hour monitoring
To compare the postoperative 24-hour analgesic requirement in the two groups.

Trial Locations

Locations (1)

ALL INDIA INSTITUTE OF MEDICAL SCIENCES; 🇮🇳 Delhi, DELHI, India

ALL INDIA INSTITUTE OF MEDICAL SCIENCES

🇮🇳Delhi, DELHI, India

SARINA K

Principal investigator

9072024026

srknandagokulum@gmail.com