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Clinical Trial Summary

The hypothesis is that the treatment with ivabradine will increase pVO2 after 16 weeks of treatment compared to baseline in the heart transplant recipient population with elevated resting HR.


Clinical Trial Description

The primary goal of this study is to assess the impact of ivabradine on cardiopulmonary exercise capacity in heart transplant recipients with elevated resting heart rate (HR).

Exercise capacity will be assessed by the determination of the peak oxygen consumption (pVO2) during standard cardiopulmonary exercise test before and after the treatment period with ivabradine. The secondary goal is to determine HR reduction with ivabradine in the patient population. ;


Study Design


Related Conditions & MeSH terms

  • Heart Transplantation, Elevated Resting Heart Rate

NCT number NCT03619187
Study type Interventional
Source Amgen
Contact
Status Withdrawn
Phase Phase 3
Start date November 2, 2018
Completion date February 19, 2020