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Left Ventricular Dysfunction clinical trials in Philadelphia, PA
3 studies for Left Ventricular Dysfunction are looking for participants at sites in and around Philadelphia (within about 30 miles). Open a study to see who can join and how to contact the study team.
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Efficacy, Safety, and Pharmacokinetics of Vericiguat in Pediatric Participants With Heart Failure Due to Left Ventricular Systolic Dysfunction (MK-1242-036)
RecruitingPhase 2/3
- Children's Hospital of Philadelphia (CHOP) ( Site 0004), Philadelphia
A Study to Learn More About How Safe Finerenone is, When it is Taken for a Longer Time With Standard Treatment, in Children and Young Adults With Heart Failure and Left Ventricular Systolic Dysfunction
RecruitingPhase 3
- Children's Hospital of Philadelphia - Cardiology, Philadelphia
- Nemours Children's Hospital - Delaware - Cardiology, Wilmington · 25 mi away
A Study to Learn More About How Well Finerenone Works, How Safe it is, and How it Moves Into, Through, and Out of the Body Compared to Placebo When Taken With Standard Treatment in Children With Heart Failure and Left Ventricular Systolic Dysfunction
RecruitingPhase 3
- Children's Hospital of Philadelphia - Cardiology, Philadelphia
- Nemours Children's Hospital - Delaware - Cardiology, Wilmington · 25 mi away
Left Ventricular Dysfunction trials in other cities
- Cleveland, OH4 studies
- New York City, NY4 studies
- Pittsburgh, PA3 studies
- Boston, MA3 studies
- Aurora, CO3 studies
- Houston, TX3 studies
- Dallas, TX3 studies
- The Bronx, NY3 studies
- Cincinnati, OH3 studies
- St. Louis, MO3 studies
- Atlanta, GA3 studies
- Ann Arbor, MI3 studies
Other studies in Philadelphia
- Cancer (all types)59 studies
- Breast Cancer56 studies
- Non-Small Cell Lung Cancer51 studies
- Metastatic Cancer46 studies
- Colorectal Cancer44 studies
- Ovarian Cancer44 studies
- Prostate Cancer44 studies
- Lung Cancer36 studies
- Acute Myeloid Leukemia34 studies
- Heart Failure31 studies
- Endometrial Cancer28 studies
- Depression26 studies
From ClinicalTrials.gov, data retrieved Oct 5, 2026. Each study sets its own eligibility; the study team decides who can join.