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NCT05222776 Clinical Trial

Predictive Values for the Outcome of Genicular Nerve Radiofrequency Ablation for Chronic Knee Pain

Osteoarthritis, Knee Clinical Trial

Official title:
Predictive Values for the Outcome of Ultrasound Guided Genicular Nerve Radiofrequency Ablation for Chronic Knee Pain

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05222776
Other study ID # 122/03
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 1, 2021
Est. completion date February 1, 2022

Study information
Verified date February 2022
Source Diskapi Teaching and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Researchers are trying to assess a predictive value or correlation between patient and procedural characteristics and outcome measures results after genicular nerve radiofrequency ablation.

Description:

Genicular nerve radiofrequency stimulation procedure is an effective treatment for patients with chronic pain due to knee osteoarthritis; however, little is known about factors that predict procedure success. This study evaluated correlation between patient characteristics and procedural characteristics and pain improvement after ultrasound guided genicular nerve radiofrequency stimulation procedure.

Recruitment information / eligibility
Status Completed
Enrollment 206
Est. completion date February 1, 2022
Est. primary completion date December 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patient's 18 years or older - Patients who recently underwent ultrasound guided genicular nerve radiofrequency (RF) procedure Exclusion Criteria: - lack of documentation of predictive factors to assess outcome - Patients in whom adequate follow-up data was not available - Patients who were prescribed a new analgesic drug or received concurrent treatments for different pain sources during the follow-up period, that could affect interpretation of genicular RF treatment results.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Turkey Diskapi Yildirim Beyazit Training and Research Hospital Ankara

Sponsors (1)
Lead Sponsor Collaborator
Diskapi Teaching and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain assessed by NRS A NRS involves asking the patient to rate his or her pain from 0 to 10 (11 point scale) with the understanding that 0 is equal to no pain and 10 is equal to worst possible pain. Change from baseline pain score at 6 months
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