Effects of Pericapsular Nerve Group Block Applied in Patients Undergoing Hip Fracture Surgery.

NCT06183541 · tracked via the Priya Life Science Turkey tracker

Sponsor

Umraniye Education and Research Hospital

Phase

Not applicable

Started

2023-11-21

Last updated

2025-11-19

Condition(s) studied

Hip FracturesPain, Postoperative

Investigational drug(s) / intervention(s)

Pericapsular Nerve Group (PENG) Block

Pericapsular Nerve Group (PENG) Block: Pericapsular nerve group (PENG) block The femoral nerve and obturator nerve terminal branches, which provide sensory innervation of the hip joint, are blocked, thus providing analgesia without creating a motor block.

Study summary

In this study, it was aimed to compare the multimodal analgesia application or the pericapsular nerve group (PENG) block methods in patients undergoing hip surgery. The effectiveness and benefit rate of the PENG block in postoperative pain will be evaluated.

Postoperative pain, need for additional analgesia, range of motion of the hip joint, mobilization time, length of hospital time and adverse events in patients undergoing hip fracture surgery with and without PENG block will be investigated.

Eligibility

Sex

ALL

Min age

30 Years

Max age

85 Years

Healthy volunteers

Inclusion Criteria: * Patients who will undergo hip fracture surgery Women and men aged 30-85 Exclusion Criteria: * Patients under 30 years old, over 85 years old * American Society of Anesthesiology (ASA) IV, * Those with cognitive impairment (alzheimer, dementia, delirium, etc.) * Those with application site infection * Those who are allergic to local anesthetic substances * Patients are non-consenting patients.

Primary outcome measure(s)

postoperative pain score — 30 min, 12th, 24th and 48th hours in the postoperative period
VAS pain score
Total opioid consumption — postoperative 48 hours
Tramadol (mg)
mobilisation time — postoperative 24-48 hours
take 5 steps with walker

Trial sites (2)

Facility	City	Region	Status
Umraniye Education and Research Hospital	Istanbul	Umraniye	Recruiting
UmraniyeERH	Istanbul	Umraniye	Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06183541 on ClinicalTrials.gov ↗ ← All trials in Turkey