Identification of Genetic Causes of Calcific Aortic Valve Disease
NCT04149600 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000
Last updated 2025-05-30
Summary
This study aims to identify the molecular genetic causes of the variability in development of calcific aortic valve disease in bicuspid and tricuspid aortic valves and their associated aortic dilation.
Conditions
- Calcific Aortic Stenosis
- Calcific Aortic Stenosis - Bicuspid Valve
- Aortic Valve Disease
- Aortic Valve Calcification
- Aortic Diseases
- Aortic Aneurysm
- Aortic Valve Cusp Abnormality
- Aortic Valve Disease Mixed
- Aortic Valve Insufficiency
Interventions
- PROCEDURE
-
Patients scheduled to undergo aortic valve replacement or aortic surgery at BIDMC will be approached for participation in this study.
Adult patients undergoing aortic valve replacement (AVR) and/or aortic resection will be enrolled.
Sponsors & Collaborators
-
Brigham and Women's Hospital
collaborator OTHER -
Beth Israel Deaconess Medical Center
lead OTHER
Eligibility
- Min Age
- 20 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2018-09-25
- Primary Completion
- 2027-06-30
- Completion
- 2027-06-30
Countries
- United States
Study Locations
More Related Trials
-
Calcium Channel Splice Variant Expression in Cardiovascular Disease and Aging
NCT00251615 ·Status: COMPLETED
-
The Genetics of Cardiomyopathy and Heart Failure
NCT00703443 ·Status: WITHDRAWN
-
Mitral Valve Prolapse (MVP) - France Study
NCT00799565 ·Status: COMPLETED ·Phase: NA
-
Study on Susceptibility Genes and Pathogenic Mechanism of Non-syndromic Familial Aortic Dissection
NCT04439565 ·Status: UNKNOWN
-
Genetic Epidemiology of CVD Risk Factors
NCT00053521 ·Status: COMPLETED
-
The BRAVE Study- The Identification of Genetic Variants Associated With Bicuspid Aortic Valve Using a Combination of Case-control and Family-based Approaches.
NCT04514445 ·Status: RECRUITING
-
Genetic Characterization of Patients With Arrhythmia-Induced Cardiomyopathy
NCT06896266 ·Status: RECRUITING
-
Genetics of Cardiovascular Disease
NCT06253481 ·Status: RECRUITING
-
Human Lipoprotein Pathophysiology - Subproject: Genetics of Familial Combined Hyperlipidemia
NCT00005313 ·Status: COMPLETED
-
Genetic Predictors of Cardiovascular Disease
NCT00339599 ·Status: COMPLETED
-
Molecular Determinants of Coronaruy Artery Disease
NCT00590291 ·Status: TERMINATED
-
Genetic Mapping of Atherogenic Lipoprotein Phenotypes
NCT00005465 ·Status: COMPLETED
-
Mapping Novel Disease Genes for Dilated Cardiomyopathy
NCT00046618 ·Status: COMPLETED
-
Genetic Basis of Abdominal Aortic Aneurysm
NCT00005526 ·Status: COMPLETED
-
Hyperapo B and Coronary Heart Disease
NCT00005168 ·Status: COMPLETED
-
The Genetic Basis of Atrial Fibrillation (AF)
NCT00248326 ·Status: COMPLETED
-
Risk Factors of Individuals With Coronary Artery Disease
NCT00260104 ·Status: UNKNOWN
-
Genetic Architecture of Plasma T-PA and PAI-1
NCT00007410 ·Status: COMPLETED
-
Vascular Disease Discovery Protocol
NCT03538639 ·Status: RECRUITING
-
Genetic Risks for Bicuspid Aortic Valve Disease
NCT01823432 ·Status: COMPLETED
-
Inflammation Genomics and Atherosclerosis - Ancillary to CARDIA
NCT00046605 ·Status: COMPLETED
-
Molecular and Morphologic Characterization of Circulating Endothelial Cells
NCT01005485 ·Status: ACTIVE_NOT_RECRUITING
-
Genetic Factors in Atherosclerosis
NCT00359307 ·Status: COMPLETED
-
Identification of Genes Expressed in Atherosclerotic Plaque
NCT00353730 ·Status: COMPLETED
-
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease
NCT00001881 ·Status: COMPLETED