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临床试验/NCT00600041
NCT00600041已完成1 期

Heart Issues of PantoPrazOle (HIPPO)

Herzzentrum Goettingen1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2005年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
20
试验地点
1
主要终点
Echocardiographic ejection fraction

研究概览

简要总结

Recently, negative inotropy of pantoprazole has been shown in isolated human myocardium. This study was designed to test the clinical relevance of this finding in healthy volunteers by measuring left ventricular function during infusion of a common intravenous high dose regimen of pantoprazole.

详细描述

Purpose: Reports on cardiac problems with oral proton pump inhibitors have caused extensive safety reviews by the U.S. Food and Drug Administration. We provide additional data on acute cardiac effects of an intravenous application.

Methods: Echocardiography was performed in 18 healthy volunteers after administration of a common high dose regimen of pantoprazole (80 mg IV bolus followed by 8 mg/h for 1h) or placebo. Design: Randomized, double-blind, placebo-controlled crossover trial.

Results: EF [%, means+/-S.E.] in the treatment group (placebo group) was 60.7+/-1.1 (61.2+/-1.7) at baseline, and 62.6+/-1.1 (62.1+/-1.9), 64.7+/-1.6 (63.5+/-1.3), 62.6+/-1.6 (61.0+/-1.6) and 63.0+/-1.4 (61.8+/-1.5) at 7.5, 15, 30 and 60 min after bolus application, respectively (p = n.s.). Similarly, no significant changes were found for cardiac output, cardiac index, blood pressure, and heart rate. In contrast, gastric pH that was used as a treatment control was significantly increased 60 min after application of pantoprazole as compared to baseline and to placebo.

Conclusions: Pantoprazole for injection is safe in healthy subjects with respect to cardiac contractile function. However, in view of recent reports of negative inotropy of the drug further studies in heart failure patients are required.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age > 18 or < 40 years
  • No signs of overt heart failure
  • Echocardiographic ejection fraction >= 55%
  • Body Mass Index 20 - 25 kg/m²
  • Excellent sonographic conditions
  • Non-smoker
  • Informed consent

排除标准

  • History of cardiac disease
  • History of other relevant pre-existing illness
  • Pathologic findings in clinical examinations
  • Pathologic echocardiographic findings
  • Pathologic ECG findings
  • Pathologic laboratory findings
  • Pregnancy and lactation
  • No or insufficient contraception
  • Intolerance of pantoprazole
  • Alcohol or drug abuse

研究组 & 干预措施

A

Experimental

Pantoprazole IV

干预措施: Pantoprazole (Drug)

B

Placebo Comparator

NaCl 0.9% IV

干预措施: Placebo (Drug)

结局指标

主要结局

Echocardiographic ejection fraction

时间窗: 60 min

次要结局

  • Cardiac index(60 min)

研究者

发起方
Herzzentrum Goettingen
申办方类型
Other

研究点 (1)

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