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临床试验/JPRN-jRCT1080222354
JPRN-jRCT1080222354已完成3 期

ZO-SA0 PhaseIII clinical trial

Zeria Pharmaceutical Co., Ltd.0 个研究点目标入组 60 人开始时间: 2014年1月6日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
60

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
>= 18age old 至 <= 74age old(—)
性别
All

入选标准

  • Patients with cardiovascular disease.
  • Out-patients who signed a written informed consent.
  • If patient age is under 20 years old, a written informed consent have to be obtained from both participant and his/her parent(s).

排除标准

  • Patients with or have a history of heart failure, renal failure, nephrotic syndrome, hepatic cirrhosis, thyroid disease
  • Patients with or have a history of lymphoedema, or patients have a history of pelvic surgery
  • Patients with allergic oedema or drug-induced oedema
  • Patients with or have a history of peripheral arterial disease, acute phlebitis, congenital vascular anomaly
  • Patients with or a history of venous thromboembolism
  • Patients who had lower leg surgery, venous sclerotherapy, or compression therapy within 4 weeks before receipt of informed consent
  • Patients who received treatment indicated for lower leg oedema, or treatment to improve lower leg oedema or subjective symptoms associated with lower leg oedema within 4 weeks before receipt of informed consent

研究者

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ZO-SA0 PhaseIII clinical trial | 临床试验