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临床试验/NCT01889966
NCT01889966已完成4 期

Vasoreactivity Testing With Intravenous Sildenafil in Patients With Precapillary Pulmonary Hypertension (Treatment Optimisation Study)

Kerckhoff Heart Center1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2013年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
10
试验地点
1
主要终点
efficacy of Sildenafil I.V. for vasoreactivity testing

研究概览

简要总结

Sildenafil is a selective pulmonary vasodilator; in patients with a special kind of pulmonary hypertension it is approved for treatment. The trial seeks to find out, whether the acute response to this treatment (= vasoreactivity testing) given intravenously is effective and allows prediction of therapy success during a following oral treatment.

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 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Precapillary pulmonary hypertension associated with connective tissue disease
  • resting mean pressure in the pulmonary artery of > 24 mmHg
  • resting mean pulmonary capillary wedge pressure (PCWP) of < 16 mmHg
  • age 18 to 80 years
  • women of childbearing potential must have a negative pregnancy test (ß-HCG in urine) and must use effective methods of contraception
  • women must not be breastfeeding
  • ability to understand and sign the informed consent, correctly signed informed consent

排除标准

  • pretreatment with Sildenafil
  • contraindications for Sildenafil treatment:
  • known intolerance to Sildenafil,
  • optic neuropathy (NAION),
  • known hereditary retina disease,
  • need of nitrate therapy
  • advanced liver cirrhosis - CHILD C
  • severely reduced renal function with GFR < 30 ml/min/1,73 m²
  • stroke or myocardial infarction within the last 6 months

研究组 & 干预措施

Sildenafil

Experimental

oral Sildenafil 20 mg three times a day for 90 days

干预措施: Sildenafil (Drug)

结局指标

主要结局

efficacy of Sildenafil I.V. for vasoreactivity testing

时间窗: 1.5 hours

Right heart catheterisation with comprehensive hemodynamic measurements (pressures in RA, RV, PA, PCW position; cardiac index (CI) by thermodilution; oxygen saturation in the PA; the same under exercise conditions) is performed. In case of precapillary pulmonary hypertension, Sildenafil is given I.V. and acute tolerability, safety and efficacy on hemodynamic parameters are registrated. Successful vasoreactivity testing is defined by lowering the mean PA pressure by 10 mmHg or more, lowering it below 40 mmHg and maintaining / rising of the CI. Safety is mainly defined by lack of a substantial effect of the study drug on systemic blood pressure.

次要结局

  • clinical efficacy of sildenafil per os predicted by testing it intravenously in the course of oral therapy(90 days)

研究者

发起方
Kerckhoff Heart Center
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. Andreas Rieth

Dr. med., senior physician cardiology

Kerckhoff Heart Center

研究点 (1)

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