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临床试验/NCT01885390
NCT01885390已完成3 期

ROX CONTROL HTN Registry: To Evaluate the ROX Coupler in Patients With Resistant or Uncontrolled Hypertension

ROX Medical, Inc.8 个研究点 分布在 3 个国家目标入组 83 人开始时间: 2014年3月1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
83
试验地点
8
主要终点
Change in ambulatory daytime mean systolic blood pressure

研究概览

简要总结

The purpose of this registry is to evaluate the safety and performance of the ROX COUPLER in patients with treatment-resistant or uncontrolled hypertension.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of resistant or uncontrolled hypertension must be made on the basis of current findings, medical history, and physical examination.

排除标准

  • Any serious medical condition that may adversely affect the patient's safety, limit the subject's ability to participate in the registry, comply with follow-up requirements, or impact the scientific integrity of the study.

结局指标

主要结局

Change in ambulatory daytime mean systolic blood pressure

时间窗: Baseline, 6 months

Change in mean ambulatory daytime systolic blood pressure at six months as compared to Baseline.

次要结局

  • Change in ambulatory daytime mean diastolic blood pressure(Baseline, 6 months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (8)

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