ACTRN12620000343909招募中未知
sability evaluation of the fit, comfort and ease of use of a novel pressure delivery device in adults with Lymphedoema
ResMed Pty. Ltd.0 个研究点目标入组 10 人开始时间: 2020年3月11日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 10
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
- Non-randomised trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •Patients who are greater than or equal to 18 years, mentally able to understand and follow the instructions of the study personnel.
- •A diagnosis of lower limb lymphoedema.
- •Established user’s pneumatic compression (must have had device for at least one (1) month).
- •Able to provide written and informed consent.
排除标准
- •Subject undergoing cancer treatment.
- •Subject has active lower limb wounds.
- •Subject is pregnant or trying to become pregnant.
- •History of pulmonary oedema or decompensated congestive heart failure.
- •Subject has any condition in which increased venous and lymphatic return is undesirable.
- •Subject has inbuilt electrical stimulator, e.g., cardiac pacemaker.
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