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临床试验/JPRN-UMIN000015587
JPRN-UMIN000015587已完成2 期

Clinical trial with NaPPS for HTLV-1-associated myelopathy (HAM) patients - Clinical trial with NaPPS for HAM patients

ReqMed Company, Ltd0 个研究点目标入组 12 人开始时间: 2014年11月3日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
12

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • (1) The person having serious complications (2) The person who received a surgical treatment within six months before clinical trial. (3) The person whose prothrombin time and the activated partial thromboplastin time is out of the inspection standard value range at the time of the screening. (4) The person who has hemorrhagic factor; with a gastric ulcer and a duodenal ulcer and gastrointestinal bleeding doubted. The person with thrombocytopenia. The person who takes anticoagulant, antiplatelet and thrombolytic medications except aspirin. (5) The person who participated in other clinical studies or a clinical trial within four months before agreement acquisition (6) The person who takes vitamin K (7) The person of the keloid constitution (8) The person with past history of drug hypersensitivity or thrombocytopenia (9) The person of alcoholism or drug dependency (10) The person who has possibility of pregnancy. (11) In addition, the person that a\the clinical trial responsibility doctor or the clinical trial allotment doctor judged the participation in this clinical trial to be inadequate

研究者

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