drugset / Trial / NCT01774656
Remission From Stage D Heart Failure
NaSingle-groupOpen-labelTreatment
Summary
The purpose of this study is to determine the proportion of subjects who have sufficient improvement in ventricular function after undergoing a standardized Left Ventricular Assist Device (LVAD) plus pharmacologic recovery treatment and testing protocol to allow removal of the LVAD within 18 months.
Timeline
- Start
- 2013-01
- Primary completion
- 2017-12
- Completion
- 2017-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Background | Carvedilol | Other / unclassified | 25 mg | — |
| Background | Digoxin | Other / unclassified | 125 g | — |
| Background | LISINOPRIL ANHYDROUS | Small molecule | 40 mg | — |
| Background | Losartan | Other / unclassified | 150 mg | — |
| Background | Spironolactone | Small molecule | 25 mg | — |