ACTRN12614000293662已完成3 期
Clinical effectiveness of Aspirin as an adjunct to compression therapy in healing chronic venous leg ulcers: a randomised double-blind placebo controlled trial
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 40
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •Eligible participants will include males and females, aged 18 years and older and have one or more leg ulcers in the presence of venous insufficiency confirmed by clinical assessment and/or duplex ultrasound.
- •The ulcer must have been present for at least six weeks.
- •Participants must have an Ankle Brachial Pressure Index [ABPI] measure of greater than or equal to 0.7 mmHg to exclude significant arterial insufficiency.
- •The eligible target ulcer will have an area of greater than or equal to 1 cm2 to less than or equal to 20 cm2 as measured by digital planimetry techniques (largest ulcer on limb and separated from other ulcers by at least 1 cm).
- •Participants must have been off aspirin for 6 weeks before coming into the study
排除标准
- •*Unable to attend scheduled treatment visits and comply with follow-up contact with study staff.
- •*Current, regular aspirin use.
- •*Aspirin intolerance.
- •*Any existing condition or treatment that is a contraindication to aspirin or to participate in the trial (decision made according to medical practitioner’s clinical judgement).
- •*Concurrent use of any other antiplatelet or anticoagulation therapy.
- •*Pregnancy or breastfeeding
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