Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/40806
Title: Comparison of conventional and cooled radiofrequency treatment of the genicular nerves versus sham procedure for patients with chronic knee pain: protocol for a multicentre, double-blind, randomised controlled trial (COGENIUS)
Authors: Vanneste, Thibaut
BELBA, Amy 
van Kuijk, Sander
Kimman, Merel
BELLEMANS, Johan 
Bonhomme, Vincent
Sommer, Micha
Emans, Pieter
Vankrunkelsven, Patrik
Tartaglia, Katrien
VAN ZUNDERT, Jan 
Issue Date: 2023
Publisher: BMJ PUBLISHING GROUP
Source: BMJ Open, 13 (8) (Art N° e073949)
Abstract: Introduction The prevalence of chronic knee pain is increasing. Osteoarthritis (OA) and persistent postsurgical pain (PPSP) are two important causes of knee pain. Chronic knee pain is primarily treated with medications, physiotherapy, life style changes and intra-articular infiltrations. A radiofrequency treatment (RF) of the genicular nerves is a therapeutical option for refractory knee pain. This study investigates the effectiveness and cost-effectiveness of conventional and cooled RF in patients suffering from chronic, therapy resistant, moderate to severe knee pain due to OA and PPSP.Methods and analysis The COGENIUS trial is a double blinded, randomised controlled trial with 2 year follow up. Patients and outcome assessors are blinded. Patients will be recruited and treated in Belgium and the Netherlands. All PPSP after a total knee prothesis and OA patients (grades 2-4) will undergo a run in period of 1-3 months where conservative treatment will be optimised. After the run in period, 200 patient per group will be randomised to conventional RF, cooled RF or a sham procedure following a 2:2:1 ratio. The analysis will include a comparison of the effectiveness of each RF treatment with the sham procedure and secondarily between conventional and cooled RF. All comparisons will be made for each indication separately. The primary outcome is the Western Ontario and McMaster Universities Osteoarthritis Index score at 6 months. Other outcomes include knee pain, physical functionality, health-related quality of life, emotional health, medication use, healthcare and societal cost and adverse events up to 24 months postintervention.Ethics and dissemination Ethics approval was obtained from the Ethics Committee of the University of Antwerp (Number Project ID 3069 Edge 002190 BUN B3002022000025), the Ethics committee of Maastricht University (Number NL80503.068.22-METC22- 023) and the Ethics committee of all participating hospitals. Results of the study will be published in international peer reviewed journals.
Notes: Vanneste, T (corresponding author), Ziekenhuis Oost Limburg, Emergency Med & Multidisciplinary Pain Ctr, Dept Anesthesiol, Intens Care Med, Genk, Belgium.; Vanneste, T (corresponding author), Maastricht Univ, Med Ctr, Dept Anesthesiol & Pain Med, Maastricht, Netherlands.
thibaut.vanneste@zol.be
Keywords: knee;pain management;chronic pain
Document URI: http://hdl.handle.net/1942/40806
ISSN: 2044-6055
e-ISSN: 2044-6055
DOI: 10.1136/bmjopen-2023-073949
ISI #: 001045474900004
Rights: Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

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