NCT01062282已完成不适用
VENIS - Prospective Observational Study of Ventavis® Inhalation Therapy in the Treatment of Patients With Pulmonary Arterial Hypertension
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Bayer
- 入组人数
- 41
- 主要终点
- The primary efficacy variable is 6-minute walking distance
研究概览
简要总结
The purpose of this study is to gain information on safety and efficacy from Korean patients who starting Ventavis treatment by observational method.
研究设计
- 研究类型
- Observational
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •The treating physician has chosen Ventavis as a suitable treatment for the patient
- •Patient with PH and classified as NYHA functional class III or IV and WHO group 1
排除标准
- •Any condition that prevents participation in the study, including pregnancy and other contraindications for Ventavis treatment (as listed in the current Ventavis patient package insert).
研究组 & 干预措施
Group 1
干预措施: Iloprost (Ventavis BAYQ6256) (Drug)
结局指标
主要结局
The primary efficacy variable is 6-minute walking distance
时间窗: At baseline and month 1,3,6 for an observational period of 6 months
次要结局
- New York Heart Association functional class(Baseline, month 1,3,6)
- PH-related symptoms and change of concomitant medication(Baseline, month 1,3,6)
- Hemodynamic parameters(If applicable ( at any time during Ventavis treatment))
- Adverse Event collection(If applicable (during the study period))
研究者
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