PENG Block & PENG PRF
ConditionOsteoarthritis (OA) of the Hip
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorAnkara City Hospital Bilkent
About this trial
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.
Eligibility criteria
Qualifiers
Presence of chronic hip pain lasting at least 3 months
Baseline Visual Analog Scale (VAS) score ≥ 4
Clinical and/or radiological diagnosis of hip osteoarthritis
Inadequate response to conservative treatments
Disqualifiers
Local or systemic infection at the intervention site
Coagulopathy or inability to discontinue anticoagulant therapy
Hip pain related to malignancy
History of previous hip arthroplasty
Trial design
Treatments tested in this trial
- PENG Block Pulsed radiofrequency
Treatment groups
84 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov