Condition
Dilated Cardiomyopathy clinical trials and research
As of November 12, 2026, Find a Trial lists 16 Dilated Cardiomyopathy clinical trials that are recruiting, at sites in 11 countries (most in United States (5), China (3), Italy (2)). By phase: Phase 1 (2), Phase 3 (1), Phase 4 (1). There are also 36 NIH-funded research projects on Dilated Cardiomyopathy, with $16.5 million in listed awards. Every study is explained in plain English. Data from ClinicalTrials.gov and NIH RePORTER, updated November 12, 2026.
- 16Clinical trials
- 36NIH research projects
- 11Countries
Newest Dilated Cardiomyopathy clinical trials
All recruiting trials (16)
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Natural history of BAG3-related dilated cardiomyopathy in Chinese adults
This is an observational study in Chinese adults with BAG3-related dilated cardiomyopathy to describe how the disease progresses over time.
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Monitoring progression of chronic cardiovascular conditions
This project will collect wearable physiologic data from adults with cardiovascular conditions to see how their heart disease changes over time.
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AZD4063 for PLN R14del dilated cardiomyopathy.
This study will test whether AZD4063 is safe and how the body processes it in adults with PLN R14del dilated cardiomyopathy.
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Identifying patients with cardiomyopathy for potential heart transplantation
This study is trying to find new ways to identify and understand cardiomyopathy in patients to better predict if they might need a heart transplant in the future.
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Predicting Ventricular Tachycardia Events in Patients with Non-Ischemic Cardiomyopathy
This study is trying to see if certain heart imaging tests can help predict the risk of dangerous heart rhythms and sudden cardiac death in people with non-ischemic cardiomyopathy.
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AI-based assessment of heart function using ECG wearable monitors
This study tests if a new AI tool using a wearable heart monitor can accurately check heart function in people with heart failure compared to traditional heart scans.
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Using AI and mobile technology to screen for dilated cardiomyopathy in family members
This study is testing if using a special mobile EKG device can help family members of people with dilated cardiomyopathy get screened for heart problems more often.
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IV donor neonatal mesenchymal stromal cells for dilated cardiomyopathy in children and young adults
We will test whether IV infusions of donor neonatal mesenchymal stromal cells can safely improve heart pumping (left ventricular ejection fraction) in children and young adults with dilated cardiomyopathy.
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Bromocriptine treatment for women with dilated cardiomyopathy
This study is testing if bromocriptine can help improve heart function in women aged 18 to 50 with dilated cardiomyopathy compared to standard treatments.
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Effects of Sirolimus on Heart Disease in Patients with a Specific Virus
This study is testing if the drug sirolimus can help improve heart health in patients with dilated cardiomyopathy who are also infected with a specific virus.
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Observing the causes and progression of cardiomyopathy
This study is trying to understand what causes cardiomyopathy and how it gets worse by collecting DNA, blood samples, and health information from people with the condition or those at risk.
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Coronary blood flow testing in people with reduced ejection fraction and left bundle branch block after CRT
This work will test whether direct intracoronary measurements of flow and pressure show reduced coronary blood flow in people with low ejection fraction and left bundle branch block who have a CRT device.
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Using cardiac MRI to assess risk in patients with dilated cardiomyopathy
This study is testing how cardiac MRI can help doctors understand the risks and better manage patients with dilated cardiomyopathy.
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A quick 10-minute heart scan for cardiac diseases
This study is testing a quick 10-minute heart scan to see if it can help diagnose heart problems better and faster for many patients without needing special dyes.
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Collecting biological samples and imaging data to study heart health and disease
This study is collecting health information and samples from people with heart conditions and healthy volunteers to learn more about heart health and disease.
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Analyzing genetic mutations in pediatric cardiomyopathy
This study is trying to learn more about the genetic causes of heart problems in children with cardiomyopathy to help improve diagnosis and treatment options for them.
NIH-funded research (36)
Early-stage science funded by the US National Institutes of Health. Most of these projects don't enroll patients, but they show what is being worked on.
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Discovery of rare genetic variants linked to dilated cardiomyopathy using big biobank data
A large-scale genetic study will look for rare gene variants that affect dilated cardiomyopathy to improve how we diagnose and manage the condition.
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Understanding how muscle ribosome mutations cause severe neonatal dilated cardiomyopathy and ways to treat it
This grant focuses on a rare genetic heart condition in newborns caused by mutations in a muscle-specific ribosomal protein, with hopes to find new ways to diagnose and treat it.
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Unlocking how rare genetic changes cause dilated cardiomyopathy
A large study will look at genetic data from many people to understand which rare variants affect dilated cardiomyopathy and how this changes risk and treatment.
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Role of Lmod2 in heart muscle and dilated cardiomyopathy
This NIH grant explores how a heart-specific protein (Lmod2) helps heart cells contract properly and how its problems can cause dilated cardiomyopathy in infants and children.
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Targeting DNA Damage Pathways in LMNA-Related Heart Disease
A study to understand how damaged DNA and inflammatory signals contribute to dilated cardiomyopathy caused by LMNA mutations and explore therapies that can protect the heart.
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Using miRNA to find new treatment paths for dilated cardiomyopathy
Researchers are studying heart-muscle disease (dilated cardiomyopathy) to discover miRNA-based clues that could lead to targeted therapies for patients.
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Skeletal muscle actin mutations and heart disease: understanding how a specific mutation affects heart function
A physician-scientist at Johns Hopkins is studying how a skeletal muscle protein mutation (ACTA1 R256H) affects heart muscle function to help people with dilated cardiomyopathy.
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Targeting immune and fibroblast crosstalk in genetic dilated cardiomyopathy
A patient-focused program aims to understand how inflammation and fibroblasts interact in genetic dilated cardiomyopathy to identify new ways to slow or stop damaging heart remodeling.
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N-terminal acetylation and heart disease in people with autism spectrum traits
This grant looks at how a specific protein modification may contribute to heart problems in people with autism, aiming to uncover targets that could reduce dangerous heart rhythms.
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CRI-103 gene therapy for dilated cardiomyopathy
A new gene therapy called CRI-103 aims to help adults with dilated cardiomyopathy by blocking a key heart-regulating protein interaction to prevent harmful heart remodeling.
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Finding why sudden cardiac death happens in dilated cardiomyopathy and how to stop it
Looks at whether genetics and heart scarring can predict and help prevent deadly heart rhythms in people with dilated cardiomyopathy.
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Understanding familial dilated cardiomyopathy to guide personalized treatments
This project will try boosting a stress-response protein called ATF4 to improve heart muscle function in people with inherited dilated cardiomyopathy.
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How dilated cardiomyopathy mutations change heart muscle myosin
Researchers will look at how inherited gene changes that cause dilated cardiomyopathy alter the structure and function of the heart’s myosin motor in people with inherited DCM.
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Using microRNA to help hearts affected by dilated cardiomyopathy
They are trying small RNA molecules to help heart muscle cells work better in people with inherited dilated cardiomyopathy.
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Understanding Lmod2's role in heart muscle and dilated cardiomyopathy
This project looks at how problems with the Lmod2 protein harm heart muscle in people with dilated cardiomyopathy and explores ways to restore its function.
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Understanding how microRNAs affect heart function in dilated cardiomyopathy
This study is looking at tiny molecules called microRNAs to see how they can help improve heart function in people with dilated cardiomyopathy, a condition that can lead to heart failure, by finding new ways to treat the genetic issues behind it.
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Understanding the causes of familial dilated cardiomyopathy to improve treatment options
This study is looking at a heart condition called familial dilated cardiomyopathy (DCM) and is testing how a protein called ATF4 can help improve heart function, with the hope of finding new treatments for people with DCM, no matter what genetic changes they have.
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How mutations in heart muscle proteins affect heart function
This study is looking at how certain genetic changes linked to dilated cardiomyopathy (DCM) affect a vital heart protein, which could help us understand heart failure better and find new treatments for people with DCM.
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DNA damage and treatments for LMNA-related dilated cardiomyopathy
This project looks at how DNA damage causes heart weakening in people with LMNA gene mutations and tests whether blocking DNA-sensing pathways can protect the heart.
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miRNA-guided approaches to find new treatments for dilated cardiomyopathy
This project looks at tiny RNA molecules in lab-grown human heart cells to find new treatment targets for people with dilated cardiomyopathy.
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Understanding heart muscle weakness from a protein defect
This work explores how a specific protein defect in heart muscle cells contributes to a common form of inherited heart weakness called dilated cardiomyopathy.
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Identifying new treatments for dilated cardiomyopathy using microRNA
This study is looking at how tiny molecules called microRNAs affect dilated cardiomyopathy, a heart condition that can lead to heart failure, to find new ways to help people with this disease feel better.
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Understanding Cell Communication in Inherited Dilated Cardiomyopathy
This research explores how heart cells communicate with each other in an inherited heart condition called dilated cardiomyopathy, using special human cells.
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Understanding how N-terminal acetylation affects heart function and arrhythmias
This study is looking at how certain genetic changes affect heart function in people with dilated cardiomyopathy and arrhythmias, using special cells from patients to better understand these conditions and find new ways to help treat them.
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Understanding how myosin affects heart function in dilated cardiomyopathy
This study is looking into how certain proteins in your heart muscle work and how we can change their activity to help improve heart function for people with dilated cardiomyopathy.
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Understanding the causes of sudden cardiac death in patients with dilated cardiomyopathy.
This study is looking at how certain genetic factors and heart changes can help doctors find out which patients with dilated cardiomyopathy are at risk for serious heart problems, so they can create better treatments and prevention plans for them.
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Finding ways to increase titin protein levels to treat heart disease.
This study is looking at how changes in a specific gene can affect heart health in people with dilated cardiomyopathy, and they're using human stem cells to find ways to boost a protein that helps the heart work better, with the hope of discovering new treatments to keep hearts strong and healthy.
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Understanding how genetic factors cause familial dilated cardiomyopathy to improve treatment options
This study is looking at a heart condition called familial dilated cardiomyopathy (DCM) and how a protein named ATF4 might help heart cells handle stress better, with the hope that boosting this protein could lead to new treatments for patients with DCM, no matter what genetic mutations they have.
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Understanding how microRNAs affect heart function in dilated cardiomyopathy
This study is looking at tiny molecules called microRNAs to see how they can help improve heart function in people with dilated cardiomyopathy, a condition that can lead to heart failure, by finding new ways to target specific genes that cause this issue.
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Understanding how protein stress affects heart function in genetic heart disease
This study is looking at how a specific stress response in heart cells might help people with Genetic Dilated Cardiomyopathy (DCM) feel better, by using heart cells made from patients' own stem cells to see how they react to problems caused by misfolded proteins.
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How mutations in heart muscle proteins affect heart function
This study looks at how certain genetic changes linked to dilated cardiomyopathy (DCM) affect a key protein in your heart that helps it pump blood, with the goal of finding out more about heart failure and helping develop better treatments for patients like you.
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Assessing genetic risk factors for dilated cardiomyopathy
This study is looking at how our genes might affect the risk of developing dilated cardiomyopathy, a serious heart condition, so that patients can get better screening and personalized treatments based on their genetic makeup.
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Using cardiac imaging to identify early signs of heart disease in families at risk
This study is looking at how special heart scans can spot early signs of dilated cardiomyopathy in family members of people who have the condition, helping to catch any changes in the heart before symptoms appear.
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Understanding heart disease caused by faulty protein signaling
This study is looking at how problems with a protein called Filamin C affect heart function in people with dilated cardiomyopathy (DCM), with the hope of finding better ways to diagnose and treat this heart condition.
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Investigating how mutations in skeletal muscle actin affect heart function in dilated cardiomyopathy
This study is looking at how a specific change in a muscle protein might affect heart function in people with dilated cardiomyopathy, with the hope of finding better treatments for those living with this condition.
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Understanding heart mechanics in patients with dilated cardiomyopathy
This study is looking at how we can better understand heart function in people with dilated cardiomyopathy (DCM) by using special ultrasound techniques, especially for those who might be at risk due to their genes, so we can catch any early signs of heart issues and tailor treatments just for them.
Related topics
Quick answers
How many Dilated Cardiomyopathy clinical trials are recruiting right now?
16, as of November 12, 2026. We update this list each time we refresh our data from ClinicalTrials.gov.
Where are these trials running?
In 11 countries. The most sites are in United States (5 trials), China (3 trials), Italy (2 trials), Denmark (1 trial), United Kingdom (1 trial). Each study page lists its sites and which ones are recruiting.
What phases are they in?
Phase 1: 2, Phase 3: 1, Phase 4: 1. Trials with no phase listed are usually device, behavioural or observational studies.
How do I join one?
Open a study, check the "Is this trial a fit for you?" section, then contact the study team listed on the page. They will ask a few screening questions. Asking is free and does not commit you to anything. Talk it over with your doctor first.
Find the studies that fit you
A list is a starting point. Tell us your situation in your own words and we'll rank the studies that match and explain why. It's free and needs no account.