Trials Sponsors Conditions Drugs Pricing

Conditions

Hip Ostearthritis

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

ultrasound-guided femoral and obturator nerve articular branches pulsed radiofrequencyProcedure

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

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

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

Sponsors & Collaborators

Diskapi Teaching and Research Hospital
Otherlead

Study Sites (1)

Ankara Etlik City Hospital

Ankara, Turkey (Türkiye)

RECRUITING

Ankara Etlik City Hospital Etlik City HospitalCONTACT(0312) 797 00 00 eminecan_02@hotmail.com

Study Officials

Gevher Rabia Genc Perdecioğlu
Diskapi TRH
STUDY CHAIR

Central Study Contacts

Emine Yuksel, TR

CONTACT

+905453489378 eminecan_02@hotmail.com

Gevher Rabia Genc Perdecioglu, TR

CONTACT

+905332009184

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

Actual (reported)

Primary Completion

April 20, 2026

Estimated (date passed)

Femoral and Obturator Nerve Articular Branches Prf

Brief Summary

Registry Overview

Trial Relationships

Study Timeline

First Submitted

Study Start

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (1)

Study Arms (1)

pulsed radiofrequency group

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

Study Officials

Central Study Contacts

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

First Submitted

Study Start

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (1)

Study Arms (1)

pulsed radiofrequency group

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

Study Officials

Central Study Contacts

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations