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临床试验/NCT02074449
NCT02074449已完成不适用

Comprehensive Characterization Of Right Ventricular Performance And Afterload In Patients With Pulmonary Arterial Hypertension Undergoing Initiation And Rapid Dose Escalation Of Treprostinil

University of Arizona1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2012年12月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
15
试验地点
1
主要终点
Measurement of change in RV coupling index on treprostinil between baseline, titration at 48-72 hours, and 3 months.

研究概览

简要总结

Patients with pulmonary arterial hypertension (PAH) are at much higher risk of death if the RV (right ventricle) is weak. The purpose of this study is to get a better understanding of the factors that determine RV adaptation and how the RV compensates on therapy. The investigator is also interested in how Remodulin (treprostinil) infused over a short period (approximately 48-72 hours) affects the patient's quality of life, medical care, and personal health behaviors.

Treprostinil, also known as Remodulin, has been approved by the US Food and Drug Administration for use in the treatment of PAH. The investigator has been treating patients with Remodulin by rapid infusion (over 48 hours) for over 6 years. The investigator would like to establish this practice as safe and effective for the benefit of other centers that treat PAH.

研究设计

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

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with clinically suspected World Health Organization (WHO) group I PAH
  • Patients with New York Heart Association/WHO functional class II-IV
  • Patients with mean pulmonary artery pressure >25 mmHg, pulmonary capillary wedge pressure </=15 mmHg, and pulmonary vascular resistance >3 wood units
  • Age >18 and <80
  • No evidence of active ischemic heart disease

排除标准

  • Left ventricular ejection fraction <50%
  • Patients with significant restrictive lung disease (FVC <60% predicted) and/or significant obstructive lung disease (FEV1 <55% predicted) within 1 year of enrollment if pulmonary function testing is available
  • Patients with significant, investigator-determined parenchymal lung disease on chest x-ray or CT of the chest
  • History of pulmonary embolism within the last three months or chronic pulmonary embolism
  • Poorly interpretable grey scale echocardiographic images
  • Contraindications to right heart catheterization
  • Moderate-severe aortic and mitral valve abnormality
  • Active or previous use of pulmonary vasoactive medication within the previous 12 weeks
  • Renal failure with serum creatinine clearance <30 ml/hr
  • High-probability ventilation-perfusion scan

结局指标

主要结局

Measurement of change in RV coupling index on treprostinil between baseline, titration at 48-72 hours, and 3 months.

时间窗: 3 months

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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