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Cryoneurolysis for the management of chronic pain in patients with knee osteoarthritis; a double-blinded randomized controlled sham trial

OBJECTIVE: Pain is the principal symptom in knee osteoarthritis (OA). Current non-operative treatment options have only moderate effects and often patients experience persistent pain or side-effects. Novel advances in the field of cryoneurolysis applies low temperatures to disrupt nerve signaling at...

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Autores principales: Nygaard, Niels-Peter Brøchner, Koch-Jensen, Carsten, Vægter, Henrik Bjarke, Wedderkopp, Niels, Blichfeldt-Eckhardt, Morten, Gram, Bibi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913284/
https://www.ncbi.nlm.nih.gov/pubmed/33637085
http://dx.doi.org/10.1186/s12891-021-04102-1
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author Nygaard, Niels-Peter Brøchner
Koch-Jensen, Carsten
Vægter, Henrik Bjarke
Wedderkopp, Niels
Blichfeldt-Eckhardt, Morten
Gram, Bibi
author_facet Nygaard, Niels-Peter Brøchner
Koch-Jensen, Carsten
Vægter, Henrik Bjarke
Wedderkopp, Niels
Blichfeldt-Eckhardt, Morten
Gram, Bibi
author_sort Nygaard, Niels-Peter Brøchner
collection PubMed
description OBJECTIVE: Pain is the principal symptom in knee osteoarthritis (OA). Current non-operative treatment options have only moderate effects and often patients experience persistent pain or side-effects. Novel advances in the field of cryoneurolysis applies low temperatures to disrupt nerve signaling at the painful area, providing pain relief. The primary aim of this randomized controlled trial (RCT) is to investigate if cryoneurolysis is superior to sham at decreasing pain intensity 2 weeks after the intervention in patients with knee OA. Secondary aims are to explore effects on pain, quality of life and functional performance over 24 months. METHODS: This two-arm, parallel-group RCT, approved by the Regional Ethics Committee, will randomly allocate patients (n = 94) to a cryoneurolysis intervention group + standardized education and exercise (CRYO) or a sham group + standardized education and exercise (SHAM) (1:1 ratio). Both groups will be assessed at baseline, 2 weeks post intervention, post education and exercise and at 6, 12 and 24 months after cryoneurolysis. The primary outcome is the NRS knee pain intensity score assessed 2 weeks post the intervention. Secondary outcome measures include functional performance (chair-stand test, 40 m walk, stair test and maximum voluntary contraction of the knee), patient reported outcomes (quality of life (EQ5D), Knee and osteoarthritis outcome scores (KOOS), among others), use of analgesics, and adverse events over 24 months. IMPACT STATEMENT: Cryoneurolysis could potentially provide an effective, safe and non-pharmacological therapeutic option to treat pain in OA patients. The potential benefits include increased functional capacity and quality of life as a result of significant pain relief and improved benefits of physical exercise. TRIAL REGISTRATION: Clinicaltrials.gov, NCT03774121, registered 3 March 2018, http://www.clinicaltrials.gov
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spelling pubmed-79132842021-03-02 Cryoneurolysis for the management of chronic pain in patients with knee osteoarthritis; a double-blinded randomized controlled sham trial Nygaard, Niels-Peter Brøchner Koch-Jensen, Carsten Vægter, Henrik Bjarke Wedderkopp, Niels Blichfeldt-Eckhardt, Morten Gram, Bibi BMC Musculoskelet Disord Study Protocol OBJECTIVE: Pain is the principal symptom in knee osteoarthritis (OA). Current non-operative treatment options have only moderate effects and often patients experience persistent pain or side-effects. Novel advances in the field of cryoneurolysis applies low temperatures to disrupt nerve signaling at the painful area, providing pain relief. The primary aim of this randomized controlled trial (RCT) is to investigate if cryoneurolysis is superior to sham at decreasing pain intensity 2 weeks after the intervention in patients with knee OA. Secondary aims are to explore effects on pain, quality of life and functional performance over 24 months. METHODS: This two-arm, parallel-group RCT, approved by the Regional Ethics Committee, will randomly allocate patients (n = 94) to a cryoneurolysis intervention group + standardized education and exercise (CRYO) or a sham group + standardized education and exercise (SHAM) (1:1 ratio). Both groups will be assessed at baseline, 2 weeks post intervention, post education and exercise and at 6, 12 and 24 months after cryoneurolysis. The primary outcome is the NRS knee pain intensity score assessed 2 weeks post the intervention. Secondary outcome measures include functional performance (chair-stand test, 40 m walk, stair test and maximum voluntary contraction of the knee), patient reported outcomes (quality of life (EQ5D), Knee and osteoarthritis outcome scores (KOOS), among others), use of analgesics, and adverse events over 24 months. IMPACT STATEMENT: Cryoneurolysis could potentially provide an effective, safe and non-pharmacological therapeutic option to treat pain in OA patients. The potential benefits include increased functional capacity and quality of life as a result of significant pain relief and improved benefits of physical exercise. TRIAL REGISTRATION: Clinicaltrials.gov, NCT03774121, registered 3 March 2018, http://www.clinicaltrials.gov BioMed Central 2021-02-26 /pmc/articles/PMC7913284/ /pubmed/33637085 http://dx.doi.org/10.1186/s12891-021-04102-1 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Study Protocol
Nygaard, Niels-Peter Brøchner
Koch-Jensen, Carsten
Vægter, Henrik Bjarke
Wedderkopp, Niels
Blichfeldt-Eckhardt, Morten
Gram, Bibi
Cryoneurolysis for the management of chronic pain in patients with knee osteoarthritis; a double-blinded randomized controlled sham trial
title Cryoneurolysis for the management of chronic pain in patients with knee osteoarthritis; a double-blinded randomized controlled sham trial
title_full Cryoneurolysis for the management of chronic pain in patients with knee osteoarthritis; a double-blinded randomized controlled sham trial
title_fullStr Cryoneurolysis for the management of chronic pain in patients with knee osteoarthritis; a double-blinded randomized controlled sham trial
title_full_unstemmed Cryoneurolysis for the management of chronic pain in patients with knee osteoarthritis; a double-blinded randomized controlled sham trial
title_short Cryoneurolysis for the management of chronic pain in patients with knee osteoarthritis; a double-blinded randomized controlled sham trial
title_sort cryoneurolysis for the management of chronic pain in patients with knee osteoarthritis; a double-blinded randomized controlled sham trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913284/
https://www.ncbi.nlm.nih.gov/pubmed/33637085
http://dx.doi.org/10.1186/s12891-021-04102-1
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