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Clinical Trials/NCT05564065
NCT05564065
Active, not recruiting
Not Applicable

Comparison of Intra-articular Steroid Injection and Radiofrequency Thermocoagulation of the Sensory Branches of the Femoral and Obdurator Nerves in Coxarthrosis Patients

Istanbul University1 site in 1 country40 target enrollmentAugust 1, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain Hip Burning
Sponsor
Istanbul University
Enrollment
40
Locations
1
Primary Endpoint
Visual Analog Scale comparison
Status
Active, not recruiting
Last Updated
3 years ago

Overview

Brief Summary

The investigators aimed that the Comparison of effectiveness of the intra-articular steroid injection and radiofrequency thermocoagulation of the sensory branches of the femoral and obdurator nerves in coxarthrosis patients

Detailed Description

Osteoarthirtis is a deficency of articular cartilge which is caused by genetic, metabolic and biochemical factors. This is a pathologic period with cartilage, bone and sinovium destruction. Pharmacological treatments and/or phsiycal medicine may not be enough to reduce pain in patients with chronic pain of osteoarthiritis. Intraarticular steroid injection is the most common used intervention method in analgesia of hip osteoarthirtis. Thus; cartilage inflammation can be decelerated and osteophyte formation can be prevented. On the other hand; because of less vascularity of hip joint, frequent steroid injections may cause aseptic necrosis. In past decades, treatment to pain of hip joint pain caused by ostheoarthrits, radiofrequency ablation treatment is used to sensory nerves which cause pain. Especially, it can be a solution in patients who do not want to undergo a surgery. Patients diagnosed with coxarthrosis will be randomly divided into two groups. One group will receive intra-articular steroid injection and the other group will receive radiofrequency thermocoagulation to the hip sensory nerve branches (femoral and obdurator). It was planned to compare the vas scores of the patients before and 1-3 months after the procedure with their effectiveness.

Registry
clinicaltrials.gov
Start Date
August 1, 2021
End Date
December 1, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Halil Cetingok

Assistant professor

Istanbul University

Eligibility Criteria

Inclusion Criteria

  • - Older than 18-year-old
  • Clincal, radiological (Grade 3-4) and laboratory examinations ara related with diagnosis of hip joint osteoarthirtis
  • Despite of previous medical and physical treatment, VAS score \> 5 and above
  • Norological examination without critical motor and sensory deficency
  • Patients who sign informed consent.

Exclusion Criteria

  • Coagulation disorders (bleeding diathesis)
  • Usage of antitrombotic, anticoagulant medications
  • Sepsis and local infection on intervention area
  • Allergic to any of drugs which is used in intervention
  • Without informed consent approval

Outcomes

Primary Outcomes

Visual Analog Scale comparison

Time Frame: 3.month

VAS is the most common pain scale. Using a ruler, the score is determined by measuring the distance (mm) on the 10-cm line between the "no pain" anchor and the patient's mark, providing a range of scores from 0-100. A higher score indicates greater pain intensity.

Study Sites (1)

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