NCT07190339

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
3mo left

Started Sep 2025

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress69%
Sep 2025Aug 2026

First Submitted

Initial submission to the registry

September 17, 2025

Completed
3 days until next milestone

Study Start

First participant enrolled

September 20, 2025

Completed
4 days until next milestone

First Posted

Study publicly available on registry

September 24, 2025

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 20, 2026

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 20, 2026

Expected
Last Updated

September 30, 2025

Status Verified

September 1, 2025

Enrollment Period

7 months

First QC Date

September 17, 2025

Last Update Submit

September 24, 2025

Conditions

Keywords

Pulsed Radiofrequency TreatmentUltrasonographyfemoral and obturator nerve articular branches

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

OTHER

femoral and obturator nerve articular branches pulsed radiofrequency for hip osteoartritis

Procedure: ultrasound-guided femoral and obturator nerve articular branches pulsed radiofrequency

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)

pulsed radiofrequency group

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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)

RECRUITING

Study Officials

  • Gevher Rabia Genc Perdecioğlu

    Diskapi TRH

    STUDY CHAIR

Central Study Contacts

Gevher Rabia Genc Perdecioglu, TR

CONTACT

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

Locations