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Study identifier: NCT07360093 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

PENG Block & PENG PRF

Condition: Osteoarthritis (OA) of the Hip  ·  Sponsor: Ankara City Hospital Bilkent

PhaseN/A
Planned participants84
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

The primary aim of this study is to prospectively compare the effects of the pericapsular nerve group (PENG) block alone and the combination of PENG block with pulsed radiofrequency (PRF) on pain intensity in patients with chronic hip pain. As a secondary aim, the effects of both treatment modalities on hip function are intended to be evaluated using valid and reliable functional assessment scales. Through this study, it is aimed to demonstrate the clinical contribution of adding PRF to the PENG block and to identify a more effective and longer-lasting approach for the interventional treatment of chronic hip pain.

This description comes directly from the study's public registry record.

Talk to the study team

Ulku Sabuncu MD, Assoc. prof.  ·  +905337085212  ·  sabuncuulku@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Ankara Bilkent City HospitalAnkara, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT07360093