Femoral and Obturator Nerve Articular Branches Prf

Not Applicable

Recruiting

• Conditions: Hip Ostearthritis

• Registration Number: NCT07190339
• Lead Sponsor: Diskapi Teaching and Research Hospital

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.

Detailed Description

Osteoarthritis of the hip joint is a common cause of pain and disability. Patients who do not respond to conservative treatments such as painkillers, physical therapy, and exercise often cannot undergo joint replacement due to comorbid conditions, while some patients prefer to postpone surgery as long as possible. Pulsed radiofrequency treatment applied to the articular branches of the femoral and obturator nerves, which innervate the joint, is a new technique for reducing hip joint pain. Previous studies have reported positive results after applying thermal neurolytic radiofrequency to the target nerves; however, this approach carries the risk of neuritis and neuroma formation. In our study, we aimed to investigate the effectiveness of pRF treatment applied to the articular branches of the femoral and obturator nerves under ultrasound guidance on pain and functionality in patients with chronic hip pain associated with osteoarthritis. The fact that the procedure is performed under ultrasound guidance, does not involve radiation exposure, and is an accessible and easy-to-perform technique makes it preferable for both patients and physicians.

Study Timeline

• Status Verified: 2025-09
• Study First Submitted: 2025-09-17
• Study First Submitted QC: 2025-09-17
• Study Start: 2025-09-20
• Study First Posted: 2025-09-24
• Last Update Submitted: 2025-09-24
• Last Update Posted: 2025-09-30
• Primary Completion: 2026-04-20
• Study Completion: 2026-08-20

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

• 1. Patients with hip and groin pain who have been diagnosed with hip osteoarthritis by direct radiography
• 2. Patients who have had hip pain above VAS 5 for more than 6 weeks
• 3. Failure of pain treatment with conservative methods such as analgesics and physical therapy

Exclusion Criteria

• 1. Patients with lumbar radiculopathy and axial back pain, sacroiliac joint, connective tissue disease
• 2. Patients who do not attend follow-up appointments regularly or cannot be reached by phone
• 3. Patients who started additional analgesic medication or underwent additional interventional procedures after the initial interventional procedure

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
numeric rating scale	Change from baseline to 2nd 6 th and 12th weeks after treatment	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"

Secondary Outcome Measures

Name	Time	Method
oxford hip score	Change from baseline to 2nd 6th and 12th weeks after treatment	The Oxford Hip Score (OHS) is a joint-specific, patient-reported outcome measure designed to assess disability in patients witth hip osteoarthritis

Trial Locations

Locations (1)

Ankara Etlik City Hospital; Ankara, Turkey (Türkiye)