A Study About the Natural History in Adults With BAG3 Dilated Cardiomyopathy (a Type of Heart Disease) (BAG3 DCM)
NCT05981092 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 35
Last updated 2025-12-11
Summary
The purpose of this study is to learn about the natural progression of DCM (dilated cardiomyopathy) caused by BAG3 gene mutations. DCM is a condition as the heart muscle is weakened and the heart becomes enlarged. This makes it hard for the heart to pump enough blood for the body.
The study is seeking up to about 35 participants who have:
* BAG3 mutation (change in the gene) that causes or is likely to cause dilated cardiomyopathy
* NYHA (New York Heart Association) Class I-IV at screening (Stage B-D)
* Left Ventricular Ejection Fraction less than or equal to 50% (meaning reduced heart function)
All participants in this study will receive their usual treatment. The investigators will observe the natural progression of people who have BAG3 DCM. This will help the investigators better understand the disease and aid in future research.
Participants will take part in this study for three years. During this time, participants will visit the site at least 8 times (about every 3 months for the first year and annually during year 2 and three). Participants will undergo study procedures and give information about their health. These procedures will include a physical exam, cardiac magnetic resonance imaging, echocardiography, ECG monitoring, activity monitoring, cardiopulmonary exercise testing, and blood tests. Participants will answer questions about health and quality of life. The study team will also call participants about 1 time over the phone.
Conditions
- Cardiomyopathy, Dilated
- Bcl-2 Anathogene-3 (BAG3) Dilated Cardiomyopathy (DCM)
Sponsors & Collaborators
-
Alexion Pharmaceuticals, Inc.
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-10-14
- Primary Completion
- 2027-08-12
- Completion
- 2027-08-12
Countries
- United States
- Netherlands
- Poland
- Spain
- United Kingdom
Study Locations
More Related Trials
-
An Integrative-"Omics" Study of Cardiomyopathy Patients for Diagnosis and Prognosis in China
NCT03076580 ·Status: UNKNOWN
-
Defining the Genetics, Biomarkers and Outcomes for Dilated Cardiomyopathy
NCT03843255 ·Status: ACTIVE_NOT_RECRUITING
-
Clinical Characteristics and Prognosis of Aortic Dissection in China (CLASSIC)
NCT05999188 ·Status: RECRUITING
-
UIC Multi-Ethnic DCM Registry
NCT07145138 ·Status: RECRUITING
-
New Diagnostic Strategy in Hypertrophic Cardiomyopathy
NCT02520856 ·Status: UNKNOWN
-
Unmasking the Prevalence of AC in an Unselected Echocardiographic Population
NCT04738266 ·Status: UNKNOWN
-
Dilated Cardiomyopathy Detection Using AI and Screening With Mobile Technology (DCM-DETECT)
NCT06688396 ·Status: RECRUITING ·Phase: NA
-
Early Identification and Treatment of Rare Cardiomyopathy Cohorts
NCT06794710 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Screening for Cardiac Amyloidosis With Nuclear Imaging for Minority Populations
NCT03812172 ·Status: COMPLETED
-
A Multi-Omics Study of Vasospastic Angina
NCT05282511 ·Status: UNKNOWN
-
Idiopathic Dilated Cardiomyopathy
NCT00005201 ·Status: COMPLETED
-
High Resolution Three-dimensional Maps of the Right Chambers in Patient Diagnosed With Cardiac Amyloidosis
NCT04956965 ·Status: UNKNOWN ·Phase: NA
-
Cardiovascular Multimodality Imaging Study
NCT06610019 ·Status: RECRUITING
-
Metabolic Characterization of Patients With Dilated Cardiomyopathy
NCT05284682 ·Status: RECRUITING
-
Diabetic/Metabolic Cardiomyopathy: Prevalence and Phenotype
NCT05181631 ·Status: UNKNOWN ·Phase: NA
-
CARdiomyopathy in Type 2 DIAbetes Mellitus
NCT04303364 ·Status: ACTIVE_NOT_RECRUITING
-
A Single-center Trial of Patients With Aortic Dissection in the Chinese XinJiang Province
NCT02378103 ·Status: UNKNOWN
-
The Chinese Hypertrophic Cardiomyopathy Study(CHCS)
NCT02696135 ·Status: RECRUITING
-
Outcome of Different Pathogenic Mutations in Hypertrophic Cardiomyopathy
NCT03726424 ·Status: UNKNOWN
-
Podocan and Wnt Pathway in the Development of Aortopathy in Bicuspid Valve Disease
NCT02806310 ·Status: COMPLETED
-
Prognostic Values of Coronary Microvascular Dysfunction in Patients With Dilated Cardiomyopathy
NCT07293338 ·Status: RECRUITING
-
The China CardioMyopathy Registry Study
NCT05871632 ·Status: NOT_YET_RECRUITING
-
Genetic Characterization of Cardiomyopathies (POLICARDIOMIO2021)
NCT05556369 ·Status: RECRUITING
-
Intracardiac Flow Assessment in Cardiac Amyloidosis
NCT05379101 ·Status: RECRUITING
-
Study of Myocardial Deformation Parameters in Patients With Hypertrophic Cardiomyopathy
NCT04112511 ·Status: COMPLETED