跳至主要内容
临床试验/NCT01593891
NCT01593891Unknown不适用

Radiographic and Intravascular (IVUS) Evaluation of Venous Morphology During CCSVI Treatment

Synergy Health Concepts, Inc.1 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2011年8月最近更新:
适应症

试验速览

阶段
不适用
入组人数
45
试验地点
1

研究概览

简要总结

Radio graphic and Intravascular (IVUS) Evaluation of Venous Morphology During Chronic Cerebral Spinal Venous Insufficiency Treatment

详细描述

To determine the safety and validity of venous angioplasty and valvuloplasty in the treatment of CCSVI. In addition, it will allow researchers to sub-classify valve morphology in relation to treatment success. This will be evidenced by venous patency forty-eight hours by Doppler ultrasound as well as clinical symptom improvement.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Retrospective

入排标准

年龄范围
20 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Ability to comprehend the nature of the study, including the risks and benefits and execute an informed consent
  • Males or Females between the ages of 20 and 60 years of age.
  • Voluntary agreement to participate in the study: Radiographic and Intravascular (IVUS) Evaluation of Venous Morphology During CCSVI Treatment.

排除标准

  • Any implantable/metallic objects that prevents subject from having a magnetic resonance imaging (MRI/MRV) study.
  • History of uncontrolled hypertension
  • Previous CCSVI treatment
  • Presence of hypercoagulable state
  • Special Populations. Special groups include, but are not limited to children, prisoners, pregnant women, fetuses, and cognitively impaired individuals who are unable to provide informed consent.

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验