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NCT04519164CompletedPhase 4

Aldosterone, the Mineralocorticoid Receptor, and Cardiovascular Disease in Obesity

Source: ClinicalTrials.gov · Last updated 15 Sept 2026

Brief summary (registry, in English)

This study will evaluate whether the mineralocorticoid receptor antagonist eplerenone, when compared to chlorthalidone plus potassium chloride, can improve cardiac MRI-derived myocardial perfusion reserve and fibrosis, independent of blood pressure, and proportionately to the severity of autonomous aldosterone production.

Status (registry)
Completed
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
79 (actual)
First submitted
17 Aug 2020
Start date
1 Dec 2020
Primary completion date
17 Sept 2025
Lead sponsor
Brigham and Women's Hospital
NCT number
NCT04519164

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 79
  • From 1 Dec 2020 to the primary completion date, 17 Sept 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Known diagnosis or treatment for type 1 or type 2 diabetes
  • Known history of CVD (myocardial infarction, heart failure, atrial fibrillation, or stroke)

Lab values

  • Serum potassium \> 5.2 mEq/L

Other

  • Estimated glomerular filtration rate \< 60 mL/min/1.73m2)
  • EKG with ischemic ST-segment or T-wave changes or Q waves in more than one territorial lead or a left bundle branch block
  • Pregnancy (verified with a pregnancy test) or breast-feeding

Who the study is looking for

  • BMI ≥ 30 with at least one of the following, or BMI ≥ 25 with at least two of the following:
    • Untreated Hypertension: Stage I (BP 120-139/80-89 mmHg) or stage II (BP 140-159/90-99 mmHg).
    • Treated Hypertension: On one anti-hypertensive medication with BP\<140/90 mmHg and willing to undergo a 2-week washout of the medication before initiating eplerenone or chlorthalidone + KCl
    • Dysglycemia: Impaired fasting plasma glucose (100-125 mg/dL) or glycated A1c 5.7-6.4%
    • Dyslipidemia: Fasting triglyceride level \> 150 mg/dL and HDL\< 40 mg/dL in men or \<50 mg/dL in women.
  • Age between 18 and 70 years old

Age in the registry: 18 years to 70 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Brigham and Women's Hospital
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.