High-dose Aldosterone Antagonist for Acute Decompensated Heart Failure
Part of paid clinical trials in San Antonio, Texas.
- Sponsor
- The University of Texas Health Science Center at San Antonio
- Study ID
- NCT02823626
- Status
- Completed
Conditions
- Acute Decompensated Heart Failure
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Spironolactone and patiromer — DRUGHigh dose spironolactone with or without patiromer based on the patient's baseline potassium
Study Details
Primary Aims 1. Evaluate the safety of high-dose spironolactone in combination of patiromer in acute decompensated heart failure patients. 2. Evaluate the efficacy of high-dose spironolactone in combination of patiromer in causing volume loss and symptom relief in patients with ADHF treated with high-dose spironolactone. Secondary Aims 1: Evaluate the effect of high-dose spironolactone on urinary sodium excretion and renal function.
Key Dates
- Start date
- Sep 30, 2016
- Status verified
- Apr 2018
- Primary completion
- Apr 30, 2018
- Completion
- Apr 30, 2018
Study Design
- Enrollment
- 48 participants (actual)
Arms
- Arm: InterventionSpironolactone and patiromer
Primary Outcome Measure
Weight loss [ Time Frame: up to 10 days ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Shweta Bansal | San Antonio | Texas | 78229 | - |
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