EUCTR2012-004117-14-GB进行中(未招募)1 期
A feasibility study to inform the design of a randomised controlled trial to identify the most clinically and cost effective length of Anticoagulation with Low molecular weight heparin In the treatment of Cancer Associated Thrombosis (ALICAT). - ALICAT
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 入组人数
- 5
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
入选标准
- •1. Receiving LMWH for treatment of CAT for five months; 2. Locally advanced or metastatic cancer; 3. Able to self-administer LMWH, or have LMWH administered by a carer; 4. Able to give informed consent; 5. Age =16 years.
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 5
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 40
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 15
排除标准
- •1.Receiving drug other than LMWH for CAT; 2.Contraindication to anticoagulation; a. known allergies to LMWHs, heparin, sulfites or benzyl alcohol, b. active major bleeding c. history of heparin-induced thrombocytopenia 3. Confirmed recurrent VTE whilst receiving anticoagulation; 4. Fitted with a prosthetic heart valve; 5. Pregnant and/or lactating females.
研究者
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