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Genicular Artery Embolisation in Patients with Osteoarthritis of the Knee (GENESIS 2): Protocol for a Double-Blind Randomised Sham-Controlled Trial

Knee osteoarthritis is a leading cause of chronic disability and economic burden. In many patients who are not surgical candidates, existing treatment options are insufficient. Clinical evidence for a new treatment approach, genicular artery embolisation (GAE), is currently limited to single arm coh...

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Autores principales: Little, Mark W., Harrison, Richard, MacGill, Sarah, Speirs, Archie, Briggs, James H., Tayton, Edward, Davies, Nev L. C., Hausen, Heike S., McCann, Claire, Levine, Lisa L., Sharma, Ricky A., Gibson, Matthew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10471661/
https://www.ncbi.nlm.nih.gov/pubmed/37337060
http://dx.doi.org/10.1007/s00270-023-03477-z
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author Little, Mark W.
Harrison, Richard
MacGill, Sarah
Speirs, Archie
Briggs, James H.
Tayton, Edward
Davies, Nev L. C.
Hausen, Heike S.
McCann, Claire
Levine, Lisa L.
Sharma, Ricky A.
Gibson, Matthew
author_facet Little, Mark W.
Harrison, Richard
MacGill, Sarah
Speirs, Archie
Briggs, James H.
Tayton, Edward
Davies, Nev L. C.
Hausen, Heike S.
McCann, Claire
Levine, Lisa L.
Sharma, Ricky A.
Gibson, Matthew
author_sort Little, Mark W.
collection PubMed
description Knee osteoarthritis is a leading cause of chronic disability and economic burden. In many patients who are not surgical candidates, existing treatment options are insufficient. Clinical evidence for a new treatment approach, genicular artery embolisation (GAE), is currently limited to single arm cohort, or small population randomised studies. This trial will investigate the use of a permanent embolic agent for embolisation of abnormal genicular arterial vasculature to reduce pain in patients with mild to moderate knee osteoarthritis. Up to 110 participants, 45 years or older, with knee pain for ≥ 3 months resistant to conservative treatment will be randomised (1:1) to GAE or a sham procedure. The treatment group will receive embolisation using 100-micron Embozene™ microspheres (Varian, a Siemens Healthineers Company) (investigational use for this indication in the UK), and the sham group will receive 0.9% saline in an otherwise identical procedure. Patients will be followed for 24 months. At 6 months, sham participants will be offered crossover to GAE. The primary endpoint is change of 4 Knee Injury and OA Outcome Score subscales (KOOS(4)) at 6 months post-randomisation. The study will also evaluate quality of life, health economics, imaging findings, and psychosocial pain outcomes. The primary manuscript will be submitted for publication after all participants complete 6 months of follow-up. The trial is expected to run for 3.5 years. Trial Registration: ClinicalTrials.gov, Identifier: NCT05423587. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00270-023-03477-z.
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spelling pubmed-104716612023-09-02 Genicular Artery Embolisation in Patients with Osteoarthritis of the Knee (GENESIS 2): Protocol for a Double-Blind Randomised Sham-Controlled Trial Little, Mark W. Harrison, Richard MacGill, Sarah Speirs, Archie Briggs, James H. Tayton, Edward Davies, Nev L. C. Hausen, Heike S. McCann, Claire Levine, Lisa L. Sharma, Ricky A. Gibson, Matthew Cardiovasc Intervent Radiol Study Protocol Knee osteoarthritis is a leading cause of chronic disability and economic burden. In many patients who are not surgical candidates, existing treatment options are insufficient. Clinical evidence for a new treatment approach, genicular artery embolisation (GAE), is currently limited to single arm cohort, or small population randomised studies. This trial will investigate the use of a permanent embolic agent for embolisation of abnormal genicular arterial vasculature to reduce pain in patients with mild to moderate knee osteoarthritis. Up to 110 participants, 45 years or older, with knee pain for ≥ 3 months resistant to conservative treatment will be randomised (1:1) to GAE or a sham procedure. The treatment group will receive embolisation using 100-micron Embozene™ microspheres (Varian, a Siemens Healthineers Company) (investigational use for this indication in the UK), and the sham group will receive 0.9% saline in an otherwise identical procedure. Patients will be followed for 24 months. At 6 months, sham participants will be offered crossover to GAE. The primary endpoint is change of 4 Knee Injury and OA Outcome Score subscales (KOOS(4)) at 6 months post-randomisation. The study will also evaluate quality of life, health economics, imaging findings, and psychosocial pain outcomes. The primary manuscript will be submitted for publication after all participants complete 6 months of follow-up. The trial is expected to run for 3.5 years. Trial Registration: ClinicalTrials.gov, Identifier: NCT05423587. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00270-023-03477-z. Springer US 2023-06-19 2023 /pmc/articles/PMC10471661/ /pubmed/37337060 http://dx.doi.org/10.1007/s00270-023-03477-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Study Protocol
Little, Mark W.
Harrison, Richard
MacGill, Sarah
Speirs, Archie
Briggs, James H.
Tayton, Edward
Davies, Nev L. C.
Hausen, Heike S.
McCann, Claire
Levine, Lisa L.
Sharma, Ricky A.
Gibson, Matthew
Genicular Artery Embolisation in Patients with Osteoarthritis of the Knee (GENESIS 2): Protocol for a Double-Blind Randomised Sham-Controlled Trial
title Genicular Artery Embolisation in Patients with Osteoarthritis of the Knee (GENESIS 2): Protocol for a Double-Blind Randomised Sham-Controlled Trial
title_full Genicular Artery Embolisation in Patients with Osteoarthritis of the Knee (GENESIS 2): Protocol for a Double-Blind Randomised Sham-Controlled Trial
title_fullStr Genicular Artery Embolisation in Patients with Osteoarthritis of the Knee (GENESIS 2): Protocol for a Double-Blind Randomised Sham-Controlled Trial
title_full_unstemmed Genicular Artery Embolisation in Patients with Osteoarthritis of the Knee (GENESIS 2): Protocol for a Double-Blind Randomised Sham-Controlled Trial
title_short Genicular Artery Embolisation in Patients with Osteoarthritis of the Knee (GENESIS 2): Protocol for a Double-Blind Randomised Sham-Controlled Trial
title_sort genicular artery embolisation in patients with osteoarthritis of the knee (genesis 2): protocol for a double-blind randomised sham-controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10471661/
https://www.ncbi.nlm.nih.gov/pubmed/37337060
http://dx.doi.org/10.1007/s00270-023-03477-z
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