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Clinical Trials/CTRI/2025/11/097105
CTRI/2025/11/097105Not yet recruitingNot Applicable

Comparison of PENG Block and Suprainguinal Fascia Iliaca Block for Facilitating Positioning in Hip Fracture Surgeries for Spinal Anesthesia: A Randomized Controlled Trial

United Institute of Medical Sciences1 site in 1 country60 target enrollmentStarted: November 18, 2025Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
60
Locations
1

Study Overview

Brief Summary

Hip fracture surgeries in elderly patients often require spinal anesthesia, but positioning these patients for the procedure can be extremely painful due to fracture-related discomfort. Adequate regional analgesia before positioning improves patient comfort and facilitates successful spinal anesthesia. This randomized controlled trial aims to compare the efficacy of Pericapsular Nerve Group (PENG) block and Suprainguinal Fascia Iliaca (SIFI) block in improving patient comfort during positioning for spinal anesthesia in hip fracture surgeries. Sixty patients scheduled for hip fracture surgery under spinal anesthesia will be randomly allocated into two equal groups to receive either a PENG block or a SIFI block using 20 mL of 0.2percent Ropivacaine under ultrasound guidance. The primary outcome will be the pain score during positioning for spinal anesthesia. Secondary outcomes will include the time for optimal positioning, change in pain scores at baseline, 15 minutes and at the time for optimal positioning, the block onset time, ease of positioning, hemodynamic changes and any noted complications. This study aims to identify which of the two regional anesthesia techniques provides superior analgesia and facilitates optimal patient positioning for spinal anesthesia in hip fracture surgeries.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Outcome Assessor Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 80.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • 1.Diagnosed with unilateral hip fracture requiring surgery under spinal anesthesia 2.ASA Physical Status I–III 3.Ability to understand and consent to the procedure.

Exclusion Criteria

  • 1.Local infection at the block site 2.Known allergy to local anesthetics 3.Coagulopathy or anticoagulant use contraindicating regional blocks 4.Altered sensorium or inability to comprehend NRS 5.Pre-existing neuropathies or chronic opioid use •Multiple fractures or polytrauma.

Investigators

Sponsor
United Institute of Medical Sciences
Sponsor Class
Private medical college
Responsible Party
Principal Investigator
Principal Investigator

Neha Sharma

United Institute of Medical Sciences, Prayagraj

Study Sites (1)

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