跳至主要内容
临床试验/NCT00159861
NCT00159861已完成3 期

A Multinational, Multi-Center, Randomised, Double-Bind, Placebo-Controlled, Parallel Group Study to Assess the Safety and Efficacy of a Subject Optimised Dose of Sildenafil Citrate (20, 40, or 80 mg. Sildenafil Citrate TID) Based on the Toleration, When Used in Combination With Intravenous Prostacyclin( Epoprostenol) in the Treatment of Pulmonary Arterial Hypertension.

Pfizer's Upjohn has merged with Mylan to form Viatris Inc.53 个研究点 分布在 11 个国家目标入组 267 人开始时间: 2003年7月1日最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
267
试验地点
53
主要终点
Categorized Change From Baseline in 6-Minute Walking Distance

研究概览

简要总结

Determination of the effects of sildenafil citrate and epoprostenol when used in combination in patients with pulmonary arterial hypertension

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Care Provider)

入排标准

年龄范围
16 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with pulmonary arterial hypertension caused by primary PAH, associated with connective tissue disease or following surgical repair of a congenital heart lesion

排除标准

  • PH other than PAH

结局指标

主要结局

Categorized Change From Baseline in 6-Minute Walking Distance

时间窗: 1 Year, 2 Year, 3 Year

Number of subjects with categorized change in 6-minute walking distance. Distance that a subject could walk in 6-minutes at a comfortable pace with as many breaks as needed. Performed as close to trough levels of sildenafil as possible (just before dosing; at least 4 hours after the previous dose of study drug). Scores for categorized changes for missing visits were imputed as the worse score of its non-missing neighbors. If a visit was missing and there was no subsequent score, the score was coded to missing.

次要结局

  • Change From Baseline in European Quality of Life (EuroQol) Visual Analogue Scale (EQ-5D VAS): Current Health State Score(Baseline, Month 15, Month 27, Month 39)
  • Change in Pulmonary Hypertension Criteria for Functional Capacity and Therapeutic Class(1 Year, 2 Year, 3 Year)
  • Change From Baseline in BORG Dyspnea Score(Baseline, Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Month 9, Month 12, Month 15, Month 18, Month 21, Month 24, Month 27, Month 30, Month 33, Month 36)
  • Survival Status(1, 2, 3, 4, and 5 years)
  • Change From Baseline in Medical Outcomes Study Short Form 36 (SF-36)(Baseline, Month 15, Month 27, Month 39)
  • Change From Baseline in European Quality of Life Scale (EuroQol) 5-Dimensions (EQ-5D): Utility Index Score(Baseline, Month 15, Month 27, Month 39)
  • Change From Baseline in Medical Outcomes Study Short Form 36 (SF-36): Reported Health Transition Score(Baseline, Month 15, Month 27, Month 39)

研究者

发起方
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (53)

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