Clinical Trial

PENG Block & PENG PRF

Study acronym: PENG-PRF
Recruiting
View on ClinicalTrials.gov →
Summary
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.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-01-14.
Status change: Not Yet Recruiting → Recruiting 2026-03-15
Trial Details
NCT Number NCT07360093
Lead Sponsor Ankara City Hospital Bilkent
Conditions Osteoarthritis (OA) of the Hip
Enrollment 84 participants
Start Date 2026-02-01
Primary Completion 2027-02-01 (estimated)
Study Completion 2027-02-28 (estimated)
Updated on ClinicalTrials.gov 2026-03-18