DRKS00013978已完成未知
Prospective, controlled trial on safety and efficacy of compression stockings for patients with CVI and pAVK (Angioflow2) - Angioflow 2
St. Josef und St. Elisabeth Hospital gGmbHKlinik für Dermatologie, Venerologie und Allergologie0 个研究点目标入组 55 人开始时间: 2018年2月9日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 55
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
- N/a: Single Arm Study
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 one(—)
- 性别
- All
入选标准
- •Age > 18 years old
- •- Chronic venous insufficiency of any genesis (varicose disease, PTS, arthrogenic congestion syndrome, dependency syndrome in obesity) in stages C3 to C5.
- •- ability to put on compression stockings or willingness to have them worn by third parties
- •- Written consent form
- •- Willingness to wear compression stockings of at least 8 hours per day during the study period
- •- Peripheral arterial occlusive disease with an ankle arm index <0.9 and >0.5 and an absolute ankle arterial pressure >60mmHg
排除标准
- •- Pregnant or nursing patient
- •- Patient participating in another treatment study Patients with severe general illness for whom there is a risk of withdrawal before the end of the study.
- •- Patient with progressive malignant disease, associated with radiation therapy, Chemotherapy or hormone therapy treated.
- •- allergy to components of the compression stocking
- •- Absolute contraindication for an compression therapy: decompensated Heart failure, septic phlebitis, Phlegmasia coerulea dolens.
- •- Acute deep or superficial leg vein thrombosis
- •- disability or reluctance, put on compression stockings or to be worn florides Ulcus cruris, C6
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