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NCT06613815

EFFECTIVENESS OF CONVENTIONAL RADIOFREQUENCY OF THE GENICULAR NERVES GUIDED BY SCOPIC VERSUS ULTRASOUND FOR THE TREATMENT OF POSTQUIRURGICAL GONALGIA

Completed Last updated 26 September 2024
What this trial tests

trial testing radiofrequency of the geniculate nerves in Knee Osteoarthritisorconventional Radiofrequencyandgeniculated Nerves in 57 participants. Completed in 31 January 2024.

Timeline
1 January 2019
Primary endpoint
31 January 2024
31 January 2024

Quick facts

Lead sponsorFundación Pública Galega Instituto de Investigación Sanitaria.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment57
Start date1 January 2019
Primary completion31 January 2024
Estimated completion31 January 2024
Sites1 location across Spain

Drugs / interventions tested

Conditions studied

Sponsor

Fundación Pública Galega Instituto de Investigación Sanitaria.

Who can join

18 and older, any sex, with Knee Osteoarthritisorconventional Radiofrequencyandgeniculated Nerves. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Knee osteoarthritis is one of the most common joint conditions in the elderly population, characterized by causing pain, stiffness and functional disability in a significant number of cases. Retrospective, non-randomized observational study, between January 2019 and January 2024, comparing the analgesic effectiveness of conventional radiofrequency of the geniculate nerves performed in a cohort of patients with a scopy-guided technique (scopic group, N=19) versus the ultrasound-guided technique (US group, N=38) in patients referred to the pain unit for chronic gonalgia of moderate-severe intensity after knee surgery. The main variable studied was the measurement of pain intensity according to the numerical rating scale (NRS) before performing the technique and at 3, 6 and 12 months after radiofrequency denervation of the geniculate nerves. Conventional radiofrequency of the geniculate nerves of the knee significantly reduces pain intensity over a period of at least 6 to 12 months in patients with chronic postoperative gonalgia, with the ultrasound-guided technique presenting the lowest scores on the numerical pain scale. It is a simple technique to perform and with few adverse effects, which allows patients to reduce the dose of opioid drugs they take chronically.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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