Femoral and Obturator Nerve Articular Branches Prf
A Study on the Effectiveness of Pulsed Radiofrequency Treatment Applied to the Femoral and Obturator Nerve Articular Branches Under Ultrasound Guidance in Chronic Hip Osteoarthritis
1 other identifier
interventional
40
1 country
1
Brief Summary
In our clinic, patients undergoing pulsed radiofrequency treatment of the femoral and obturator nerve articular branches under ultrasound guidance for pain management due to hip and groin pain associated with hip osteoarthritis will have the efficacy of these methods on pain compared with the Numeric Rating Scale (NRS) and Oxford Hip Score (OHS) at 2, 6, 12 weeks.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Sep 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 17, 2025
CompletedStudy Start
First participant enrolled
September 20, 2025
CompletedFirst Posted
Study publicly available on registry
September 24, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 20, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
August 20, 2026
ExpectedSeptember 30, 2025
September 1, 2025
7 months
September 17, 2025
September 24, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
numeric rating scale
The numeric rating scale (NRS) is a pain screening tool, commonly used to assess pain severity at that moment in time using a 0-10 scale, with zero meaning "no pain" and 10 meaning "the worst pain imaginable"
Change from baseline to 2nd 6 th and 12th weeks after treatment
Secondary Outcomes (1)
oxford hip score
Change from baseline to 2nd 6th and 12th weeks after treatment
Study Arms (1)
pulsed radiofrequency group
OTHERfemoral and obturator nerve articular branches pulsed radiofrequency for hip osteoartritis
Interventions
Hemodynamic monitoring is provided. The hip joint where the procedure will be performed is cleaned with povidone-iodine. Sterile draping is performed. For PRF application to the articular branches of the femoral nerve, a convex ultrasound probe is first used to locate the articular branches of the femoral nerve in the groin area, followed by the articular branches of the obturator nerve. The radiofrequency cannula is inserted sequentially into the target points and sensory feedback is obtained. Then, a pulsed radiofrequency current, which has therapeutic properties for chronic pain and does not damage tissues by exceeding a temperature of 42 degrees, is applied to the relevant nerve root for 240 seconds. Subsequently, an injectate consisting of 2 cc of 5% bupivacaine, 4 mg of dexamethasone, and 2 cc of physiological saline is administered to the same nerve. Translated with DeepL.com (free version)
Eligibility Criteria
You may qualify if:
- \. Patients with hip and groin pain who have been diagnosed with hip osteoarthritis by direct radiography
- \. Patients who have had hip pain above VAS 5 for more than 6 weeks
- \. Failure of pain treatment with conservative methods such as analgesics and physical therapy
You may not qualify if:
- \. Patients with lumbar radiculopathy and axial back pain, sacroiliac joint, connective tissue disease
- \. Patients who do not attend follow-up appointments regularly or cannot be reached by phone
- \. Patients who started additional analgesic medication or underwent additional interventional procedures after the initial interventional procedure
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ankara Etlik City Hospital
Ankara, Turkey (Türkiye)
Study Officials
- STUDY CHAIR
Gevher Rabia Genc Perdecioğlu
Diskapi TRH
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Supervisor Investigator
Study Record Dates
First Submitted
September 17, 2025
First Posted
September 24, 2025
Study Start
September 20, 2025
Primary Completion
April 20, 2026
Study Completion (Estimated)
August 20, 2026
Last Updated
September 30, 2025
Record last verified: 2025-09