设计下肢静脉溃疡的多臂、多阶段平台试验——下肢静脉溃疡:管理和根除,静脉平台研究。设计静脉性腿部溃疡(VLU)的平台/适应性试验-静脉平台。

NIHR open research Pub Date : 2025-04-14 eCollection Date: 2025-01-01 DOI:10.3310/nihropenres.13847.1
Sarah Onida, Alun Huw Davies
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引用次数: 0

摘要

背景:下肢静脉性溃疡(VLU)是最严重的静脉疾病,是患者和社会的重要负担。VLU的治疗方法有很多,包括伤口治疗、药物治疗和手术干预。然而,支持腿部溃疡治疗的高水平随机试验数据缺乏,限制了其在临床实践中的采用。我们开发了一个平台试验,评估VLU的多种干预措施,包括多个多臂多阶段试验。方法:在五个工作流程中进行范围审查、调查、会议和焦点小组,以告知拟议平台试验的发展。我们邀请了国际静脉疾病专家、有VLU生活经验的患者、对VLU护理感兴趣的医疗保健专业人员、方法学家、行业合作伙伴和其他关键利益相关者参与,以帮助确定优先研究领域和方法学,并最终确定拟议的试验设计。结果:基于这一反馈,拟议的多臂多阶段(MAMS)平台试验将在三个患者领域进行:活动性溃疡存在时间少于6个月的患者(领域1),活动性溃疡存在时间超过6个月的患者(领域2)和溃疡愈合的患者(领域3)。干预措施包括伤口护理、药物治疗、浅表静脉回流的干预,以及社区、初级和二级医疗机构提供的监测策略。结论:我们的MAMS平台试验开发突出了方法开发和此类研究的潜在交付方面的许多挑战和机遇。在我们的工作流程中进行的工作将有助于为该领域的未来研究提供信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Designing a multi-arm, multi-stage platform trial for venous leg ulceration - Venous leg ulcers: management and eradication, the VEIN platform study.: Designing a platform/adaptive trial for venous leg ulcers (VLU) - The VEIN platform.

Background: Venous leg ulceration (VLU) is the most severe form of venous disease and an important burden to patients and society. Many treatments for VLU exist, including wound therapies, medications, and surgical interventions. However, high-level randomized trial data supporting leg ulcer treatments are lacking, limiting their adoption in clinical practice. We developed a platform trial assessing multiple interventions for VLU comprising multiple multi-arm multi-stage trials.

Methods: Scoping reviews, surveys, meetings, and focus groups were conducted over five work streams to inform the development of the proposed platform trial. We involved international experts in venous disease, patients with a lived experience of VLU, healthcare professionals with an interest in VLU care, methodologists, industry partners, and other key stakeholders to help inform priority research areas and methodology, and finalize the proposed trial design.

Results: Based on this feedback, the proposed multi-arm multi-stage (MAMS) platform trial will be delivered across three patient domains: patients with active ulceration present for less than six months (Domain 1), patients with active ulceration present for more than six months (Domain 2), and patients with healed ulceration (Domain 3). Interventions included wound care, medication, intervention for superficial venous reflux, and surveillance strategies delivered across community, primary, and secondary care.

Conclusions: Our MAMS platform trial development highlighted many challenges and opportunities in methodology development and the potential delivery of such a study. The work performed in our work streams will help inform future research in this field.

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