NCT06751472

Brief Summary

It has been observed that the deterioration in the physical performance of the hip, the medical need before the specialist consultation and the deterioration in the health status can progress treatment\[3\]. When conservative treatment methods such as physical therapy and weight change, the use of walking aids (such as a cane) and analgesic agents are used, these interruptions usually provide short-term and partial benefits. After the application of medical treatment procedures, hip prostheses are usually separated. However, the additional diseases of the patients, the fact that the surgery is a major surgery and the mortality rate is high, and the life of the prostheses used are limited have led to the search for alternative pain palliation. Hip joint radiofrequency thermocoagulation is a procedure performed in our clinic. In this study, we aimed to examine the long-term effects of hip RFT on pain and functional capacity changes in patients.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
76

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jan 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
not yet 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

First Submitted

Initial submission to the registry

December 23, 2024

Completed
7 days until next milestone

First Posted

Study publicly available on registry

December 30, 2024

Completed
6 days until next milestone

Study Start

First participant enrolled

January 5, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 20, 2025

Completed
Last Updated

December 30, 2024

Status Verified

December 1, 2024

Enrollment Period

2 months

First QC Date

December 23, 2024

Last Update Submit

December 25, 2024

Conditions

Keywords

chronic hip painradiofrequency thermocoagulationArticular Branches of the Femoral and Obturator Nerve

Outcome Measures

Primary Outcomes (1)

  • chronic pain assessment

    Pain will be assessed with the SAS (Verbal Pain Score) score before surgery, at 12 and 24 months.

    12 month, 24 month

Secondary Outcomes (1)

  • functional capacity assesment

    12 month, 24 month

Study Arms (1)

RFT

Conventional radiofrequency thermocoagulation (RFT) procedure was applied to the femoral and obturator nerve joint branches electively due to chronic hip pain.

Diagnostic Test: VPS (Verbal Pain Score)Diagnostic Test: WOMAC (Western Ontario and McMaster Universities Arthritis Index) scale

Interventions

İt is a pain intensity determination system based on the system where there person tells a point between 0=(no pain) 10=( unbearable pain) and to describe their pain

RFT

It includes 24 questions under three sub-headings as pain, stiffness and physical function

RFT

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients who underwent conventional RF will be included in the prospective studies titled "Treatment of chronic hip pain with conventional radiofrequency thermocoagulation to the articular branches of the femoral and obturator nerves" and "Comparison of conventional radiofrequency thermocoagulation to the articular branches of the femoral and obturator nerves with intra-articular steroid injection and pericapsular nerve group (PENG) block in chronic hip pain" (theses of assistant Sevilay Şimşek Karaoğlu and Bilge Ergün, respectively) conducted in our clinic.

You may qualify if:

  • Being over 18 years of age
  • Having received written consent
  • Those with chronic hip pain lasting longer than 3 weeks

You may not qualify if:

  • Major psychiatric disease
  • Patients with lumbar pressure pain or referred pain
  • Patients using anticoagulant agents
  • Patients with infection in the area to be treated
  • Those with local anesthetic allergy
  • Those with betamethasone allergy
  • Pregnant women

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Adnan Menderes University, Research hospital

Aydin, 09100, Turkey (Türkiye)

Location

Central Study Contacts

Sinem Sarı, Prof,MD

CONTACT

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Aydin Adnan Menderes University

Study Record Dates

First Submitted

December 23, 2024

First Posted

December 30, 2024

Study Start

January 5, 2025

Primary Completion

March 1, 2025

Study Completion

April 20, 2025

Last Updated

December 30, 2024

Record last verified: 2024-12

Locations