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NCT03816124 Clinical Trial

The Effect of Radiofrequency Ablation of Genicular Nerves on Postural Stability in Patients With Knee Osteoarthritis

Osteoarthritis, Knee Clinical Trial

Official title:
The Effect of Radiofrequency Ablation of Genicular Nerves on Postural Stability in Patients With Knee Osteoarthritis

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT03816124
Other study ID # 09.2018.663
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date December 1, 2018
Est. completion date December 2019

Study information
Verified date January 2019
Source Marmara University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In advanced knee osteoarthritis, postural stability is also disturbed. There are some concerns about performing radiofrequency ablation to genicular nerves since this may further decrease the postural stability of the patient. The aim of this study is to see if application of genicular radiofrequency causes a significant change in postural stability.

Recruitment information / eligibility
Status Recruiting
Enrollment 30
Est. completion date December 2019
Est. primary completion date June 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Stage 3 and 4 knee osteoarthritis according to Kellgren-Lawrance scale

- Knee pain more than 3 months

Exclusion Criteria:

- Neurological diseases such as polyneuropathies

- Presence of severe psychiatric disorders

- Hemodynamic instability

- History of any surgery from the knee

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• radiofrequency ablation
radiofrequency ablation of the genicular nerves

Locations
Country Name City State
Turkey Marmara University School of Medicine Department of Physical Medicine and Rehabilitation Istanbul

Sponsors (1)
Lead Sponsor Collaborator
Marmara University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Visual analogue scale The change of pain will be evaluated with 10 cm visual analogue scale will be applied to the patients, 0 being no pain while 10 being intolerable pain 3 weeks and 3 months after the intervention
Secondary Postural stability The change of weight bearing indexes of both feet will be measured 3 weeks and 3 months after the treatment
Secondary WOMAC Western Ontario & McMaster Universities Osteoarthritis Index 3 weeks and 3 months after the treatment
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