NCT00878943No Longer Available不适用
A Local, Multi-centre, Open Label Access Study, To Provide Sildenafil Therapy To Eligible Adult Patients With Pulmonary Arterial Hypertension Completing A1481244 Study In India Or Ongoing In A1481269 Study Who Continue To Receive Benefit From Sildenafil Therapy.
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.5 个研究点 分布在 1 个国家开始时间: 2009年4月9日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- No Longer Available
- 发起方
- 试验地点
- 5
研究概览
简要总结
In an earlier study, sildenafil citrate administered to patients of PAH led to improvement in pulmonary arterial pressure, cardiac output, quality of life, and other parameters as compared to placebo. This protocol provides mechanism for patients who have clinical deterioration on other PAH approved therapies to have access to sildenafil prior to marketing authorization in India.
研究设计
- 研究类型
- Expanded Access
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
- •Subject who complete the A1481244 study and require Sildenafil (Revatio TM) 20 mg TID therapy.
- •All women of childbearing potential must use adequate contraception throughout the study and four weeks after completion of the study
排除标准
- •Pregnant or lactating women
- •Participation in other studies during study participation
- •Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation
研究者
研究点 (5)
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