Mineralocorticoid Receptor Antagonism Clinical Evaluation in Atherosclerosis Trial

PHASE4CompletedINTERVENTIONAL
Enrollment

79

Participants

Timeline

Start Date

January 31, 2016

Primary Completion Date

April 29, 2022

Study Completion Date

April 29, 2022

Conditions
Atherosclerosis
Interventions
DRUG

Spironolactone

Patients will be given Spironolactone 12.5 mg on week 0 (visit 2). Patients will be escalated to 25 mg daily Spironolactone or maximal tolerated dose over a 4-week period. Patients will continue treatment for an additional 48 weeks.

DRUG

Placebo

Placebo

Trial Locations (1)

44106

University Hospitals Cleveland Medical Center, Cleveland

All Listed Sponsors
collaborator

University of Maryland

OTHER

collaborator

University of Toronto

OTHER

collaborator

Winthrop University

OTHER

lead

University Hospitals Cleveland Medical Center

OTHER

NCT02169089 - Mineralocorticoid Receptor Antagonism Clinical Evaluation in Atherosclerosis Trial | Biotech Hunter | Biotech Hunter