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膝关节骨关节炎患者的膝关节动脉栓塞术(GENESIS 2):一项双盲随机假对照试验的方案。

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

机构信息

University Department of Radiology, Royal Berkshire Hospital, London Road, Reading, RG1 5AN, UK.

Centre for Integrative Neuroscience and Neurodynamics, University of Reading, Reading, UK.

出版信息

Cardiovasc Intervent Radiol. 2023 Sep;46(9):1276-1282. doi: 10.1007/s00270-023-03477-z. Epub 2023 Jun 19.

Abstract

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) 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.

摘要

膝关节骨关节炎是导致慢性残疾和经济负担的主要原因。对于许多不符合手术条件的患者,现有的治疗选择是不够的。一种新的治疗方法——膝下动脉栓塞术(GAE)的临床证据目前仅限于单臂队列或小人群随机研究。本试验将研究使用永久性栓塞剂栓塞异常的膝下动脉血管结构,以减轻轻度至中度膝关节骨关节炎患者的疼痛。多达 110 名年龄在 45 岁及以上、膝关节疼痛持续 3 个月以上且对保守治疗有抵抗的患者将被随机(1:1)分为 GAE 组或假手术组。治疗组将接受 100 微米 Embozene™微球(Varian,西门子 Healthineers 公司)栓塞(在英国,该产品用于该适应症的研究性使用),假手术组将接受 0.9%生理盐水进行其他相同的操作。患者将接受 24 个月的随访。在 6 个月时,假手术组将被提供交叉治疗转为 GAE 组。主要终点是随机分组后 6 个月时 4 项膝关节损伤和骨关节炎结局评分(KOOS)子量表的变化。该研究还将评估生活质量、健康经济学、影像学发现和心理社会疼痛结局。所有参与者完成 6 个月的随访后,将提交主要手稿进行发表。预计试验将持续 3.5 年。试验注册:ClinicalTrials.gov,标识符:NCT05423587。

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State of the evidence.证据状况。
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