Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
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Status: Not yet recruiting

Baxdrostat and Ventricular Remodeling

The goal of this trial is to learn whether adding the blood pressure medication baxdrostat (Baxfendy) to standard-of-care medical therapies will beneficially change the heart structure and function of adults who have high blood pressure, thickened left heart walls, and are at risk for heart or kidney disease. To determine if baxdrostat improves heart structure and function, the participants will: * take a baxdrostat or a placebo (a look-alike tablet that contains no drug) tablet once a day for 12 months * undergo a safe and non-invasive cardiac magnetic resonance imaging scan (to measure heart mass, stiffness and function) at the beginning of the study and 12 months later * visit the clinic for checkups and blood or urine tests 2 weeks, 1 month, 3 months, 6 months, 9 months and 12 months after taking the first tablet

Participants needed: 286
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Subodh VermaUpdated: Jun 17, 2026Locations: 2
Eligibility criteria

Individuals ≥18 years of age who are willing and able to provide signed informed... [+56]

Status: Not yet recruiting

Finerenone and Cardiac Remodeling

The goal of this clinical trial is to learn if the drug finerenone (Karendia) can improve heart function in participants who are at risk for heart and kidney disease. The main question it aims to answer is whether adding finerenone to standard-of-care heart failure medical therapies will beneficially alter the heart structure and function of people who have risk factors for heart and kidney complications and whose left side of the heart is enlarged. The researchers will compare finerenone to a placebo (a look-alike substance that contains no drug) to see if finerenone improves heart structure and function. Participants will: * take a finerenone or a placebo tablet once a day for 12 months * have a cardiac magnetic resonance imaging (cMRI; a safe, non-invasive scan to measure heart mass, stiffness and function) test at the beginning of the study and 12 months later * visit the clinic after one, three, six and twelve months to assess overall health and/or perform blood or urine tests

Participants needed: 156
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Subodh VermaUpdated: Dec 8, 2025Locations: 3
Eligibility criteria

Individuals ≥18 years of age who are willing and able to provide signed informed... [+15]

Females who are planning to become pregnant, are breastfeeding or are planning t... [+29]

Status: Not yet recruiting

SGLT2 Inhibition With Empagliflozin in Fontan Circulatory Failure

Some people are born with a birth defect where they only have one functioning ventricle (lower chamber) in their heart. This condition can be initially managed with a Fontan operation, but there is a risk of developing Fontan Circulatory Failure (FCF) later in life. FCF occurs when the single working heart ventricle is no longer strong enough to pump blood throughout the body. This also means the heart has difficulty supplying oxygen to keep up with the needs of the body. As a result, individuals living with FCF may have some challenges carrying out day to day activities. A heart transplant is currently the only therapeutic option for individuals living with FCF. The investigators are conducting this trial to determine whether a medication called empagliflozin can help these people have a better quality of life.

Participants needed: 410
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Subodh VermaUpdated: May 2, 2025Locations: 1
Eligibility criteria

Adults (≥18 years of age) with FCF, defined by dysfunction of the Fontan physiol...

Diuretic initiation or dose change ≤2 weeks prior to enrollment On a SGLT2 inhib... [+20]