Marfan syndrome
Marfan syndrome
Explore linked clinical trials. Standard reference: MONDO:000794716 results · Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Pregnancy in Women With Rare Multisystemic Vascular Diseases: COGRare5 Study | Abnormalities, Multiple, Bone Diseases, Developmental, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, Marfan syndrome, Skin and Connective Tissue Diseases, arteriovenous hemangioma/malformation, bone disorder, cardiovascular disorder, central nervous system disorder, congenital heart disease, connective tissue disorder, heart disorder, hematologic disorder, hemorrhagic disease, hereditary disease, hereditary hemorrhagic telangiectasia, lymphatic system disorder, lymphedema, musculoskeletal system disorder, nervous system disorder, telangiectasis, vascular disorder, vascular hemostatic disease, vascular malformation | Recruiting | Not stated | 2026-09-28 | NCT04194619 | |
| ScATtEred Rare Disease Biobanks: a Model of Sample/Data Collection With susTainablE and Shared Criteria | Abnormalities, Multiple, Bone Diseases, Developmental, Cardiovascular Abnormalities, Cognition Disorders, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Dyskinesias, Huntington disease, Hypersensitivity, Immediate, Marfan syndrome, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Rare Diseases, Skin and Connective Tissue Diseases, angioedema, basal ganglia disorder, bone disorder, brain disorder, cardiovascular disorder, central nervous system disorder, choreatic disease, cognitive disorder, congenital heart disease, connective tissue disorder, dementia, heart disorder, hereditary disease, immune system disorder, inherited neurodegenerative disorder, movement disorder, musculoskeletal system disorder, nervous system disorder, neurodegenerative disease, psychiatric disorder, skin disorder, skin vascular disease, urticaria, vascular disorder | Recruiting | Not stated | 2026-08-27 | NCT06782230 | |
| PregnAncy-Related Aortic DISsEction in China | Abnormalities, Multiple, Acute Aortic Syndrome, Aneurysm, Aortic Dissection, Bone Diseases, Developmental, Cardiovascular Abnormalities, Collagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, Dissection, Blood Vessel, Ehlers-Danlos syndrome, Ehlers-Danlos syndrome, vascular type, Female Urogenital Diseases and Pregnancy Complications, Hemic and Lymphatic Diseases, Loeys-Dietz syndrome, Marfan syndrome, Musculoskeletal Abnormalities, Skin Abnormalities, Skin and Connective Tissue Diseases, Urogenital Diseases, aortic aneurysm, aortic disorder, bone disorder, cardiovascular disorder, congenital heart disease, connective tissue disorder, heart disorder, hematologic disorder, hemorrhagic disease, hereditary disease, hereditary skin disorder, musculoskeletal system disorder, pregnancy disorder, skin disorder, vascular disorder, vascular hemostatic disease | Recruiting | Not stated | 2026-07-17 | NCT07672210 | |
| Transcriptomic Study of Adult Population With Marfan Syndrome | Abnormalities, Multiple, Aneurysm, Bone Diseases, Developmental, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Marfan syndrome, Skin and Connective Tissue Diseases, aortic aneurysm, aortic disorder, bone disorder, cardiovascular disorder, congenital heart disease, connective tissue disorder, heart disorder, hereditary disease, musculoskeletal system disorder, thoracic aortic aneurysm, vascular disorder | Active, not recruiting | Not stated | 2026-07-02 | NCT05700175 | |
| Fibroblasts and Thoracic Aortic Aneurysms: in Vitro Characterization in With Marfan Syndrome and Genetic Aortic Diseases | Abnormalities, Multiple, Aneurysm, Bone Diseases, Developmental, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Marfan syndrome, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Rare Diseases, Skin and Connective Tissue Diseases, aortic aneurysm, aortic disorder, bone disorder, cardiovascular disorder, congenital heart disease, connective tissue disorder, heart disorder, hereditary disease, musculoskeletal system disorder, thoracic aortic aneurysm, vascular disorder | Enrolling by invitation | Not stated | 2026-05-28 | NCT06786754 | |
| National Network for Cardiovascular Genomics: Advancing Cardiovascular Healthcare for Hereditary Diseases in Brazil's Unified Health System Through a Multicenter Registry | Abnormalities, Multiple, Aneurysm, Aortic Dissection, Arrhythmias, Cardiac, Bone Diseases, Developmental, Brugada syndrome, Cardiac Conduction System Disease, Cardiomegaly, Cardiovascular Abnormalities, Collagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, Death, Death, Sudden, Death, Sudden, Cardiac, Dissection, Blood Vessel, Dyslipidemias, Ehlers-Danlos syndrome, Ehlers-Danlos syndrome, vascular type, Hemic and Lymphatic Diseases, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Loeys-Dietz syndrome, Marfan syndrome, Musculoskeletal Abnormalities, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Polymorphic Catecholaminergic Ventricular Tachycardia, Skin Abnormalities, Skin and Connective Tissue Diseases, Tachycardia, aortic aneurysm, aortic disorder, aortic valve disorder, aortic valve stenosis, arrhythmogenic right ventricular cardiomyopathy, bone disorder, cardiac arrest, cardiomyopathy, cardiovascular disorder, congenital heart disease, connective tissue disorder, dilated cardiomyopathy, familial hypercholesterolemia, heart disorder, heart valve disorder, hematologic disorder, hemorrhagic disease, hereditary disease, hereditary skin disorder, hyperlipidemia, hyperlipoproteinemia, hypertrophic cardiomyopathy, inborn errors of metabolism, laminopathy, metabolic disease, musculoskeletal system disorder, non-compaction cardiomyopathy, restrictive cardiomyopathy, short QT syndrome, skin disorder, subvalvular aortic stenosis, vascular disorder, vascular hemostatic disease, ventricular tachycardia | Recruiting | Not stated | 2026-05-08 | NCT06546137 | |
| Nutritional Ketosis Marfan | Abnormalities, Multiple, Acute Aortic Syndrome, Aneurysm, Aortic Dissection, Bone Diseases, Developmental, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dissection, Blood Vessel, Marfan syndrome, Skin and Connective Tissue Diseases, aortic disorder, bone disorder, cardiovascular disorder, congenital heart disease, connective tissue disorder, heart disorder, hereditary disease, musculoskeletal system disorder, vascular disorder | Not yet recruiting | Not applicable | 2026-03-27 | NCT07495267 | |
| Biological Collection for Marfan and Related Syndromes | Abnormalities, Multiple, Bone Diseases, Developmental, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Marfan syndrome, Skin and Connective Tissue Diseases, bone disorder, cardiovascular disorder, congenital heart disease, connective tissue disorder, heart disorder, hereditary disease, musculoskeletal system disorder | Recruiting | Not stated | 2026-03-17 | NCT04970459 | |
| Adapted Physical Activity Program (APA) for Effort Rehabilitation of Children and Teenagers With Marfan Syndrome | Abnormalities, Multiple, Bone Diseases, Developmental, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Marfan syndrome, Skin and Connective Tissue Diseases, bone disorder, cardiovascular disorder, congenital heart disease, connective tissue disorder, heart disorder, hereditary disease, musculoskeletal system disorder | Recruiting | Not applicable | 2026-03-03 | NCT05838235 | |
| Clinical and Psychosocial Factors Associated With Physical Activity Level in Adults With Marfan Syndrome | Abnormalities, Multiple, Bone Diseases, Developmental, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Fatigue, Kinesiophobia, Marfan syndrome, Neurologic Manifestations, Pain, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Skin and Connective Tissue Diseases, anxiety disorder, bone disorder, cardiovascular disorder, congenital heart disease, connective tissue disorder, heart disorder, hereditary disease, musculoskeletal system disorder, phobic disorder, psychiatric disorder | Not yet recruiting | Not stated | 2026-02-19 | NCT07419386 | |
| Pathogenetic Basis of Aortopathy and Aortic Valve Disease | Abnormalities, Multiple, Acute Aortic Syndrome, Aneurysm, Aneurysm, Ascending Aorta, Aortic Aneurysm, Giant Congenital, Aortic Dissection, Bicuspid Aortic Valve Disease, Bone Diseases, Developmental, Cardiovascular Abnormalities, Collagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, Dissection, Blood Vessel, Dissection, Thoracic Aorta, Ehlers-Danlos syndrome, Ehlers-Danlos syndrome, vascular type, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Hemic and Lymphatic Diseases, Loeys-Dietz syndrome, Male Urogenital Diseases, Marfan syndrome, Musculoskeletal Abnormalities, PHACE syndrome, Sex Chromosome Disorders, Shprintzen Golberg craniosynostosis, Skin Abnormalities, Skin and Connective Tissue Diseases, Turner syndrome, Urogenital Abnormalities, Urogenital Diseases, aortic aneurysm, aortic aneurysm, familial thoracic 1, aortic disorder, aortic valve disorder, arterial tortuosity syndrome, bone disorder, cardiovascular disorder, chromosomal disorder, congenital contractural arachnodactyly, congenital heart disease, connective tissue disorder, cutis laxa, autosomal recessive, type 1A, disorder of sexual differentiation, endocrine system disorder, familial thoracic aortic aneurysm and aortic dissection, gonadal disorder, gonadal dysgenesis, heart disorder, heart valve disorder, hematologic disorder, hemorrhagic disease, hereditary disease, hereditary skin disorder, musculoskeletal system disorder, sex chromosome disorder of sex development, skin disorder, thoracic aortic aneurysm, vascular disorder, vascular hemostatic disease | Active, not recruiting | Not stated | 2026-02-13 | NCT03440697 | |
| Complex Aortic Aneurysm Repair Using Physician Modified Endografts and Custom Made Devices | Abnormalities, Multiple, Acute Aortic Syndrome, Aneurysm, Aneurysm, Aortic Arch, Aortic Dissection, Bone Diseases, Developmental, Cardiovascular Abnormalities, Collagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, Dissection, Blood Vessel, Ehlers-Danlos syndrome, Hemic and Lymphatic Diseases, Loeys-Dietz syndrome, Marfan syndrome, Musculoskeletal Abnormalities, Skin Abnormalities, Skin and Connective Tissue Diseases, abdominal aortic aneurysm, aortic aneurysm, aortic disorder, bone disorder, cardiovascular disorder, congenital heart disease, connective tissue disorder, heart disorder, hematologic disorder, hemorrhagic disease, hereditary disease, hereditary skin disorder, musculoskeletal system disorder, skin disorder, thoracic aortic aneurysm, vascular disorder, vascular hemostatic disease | Recruiting | Not applicable | 2025-10-22 | NCT02050113 | |
| Multicentre Longitudinal Study of Bone Mineralisation Characteristics in Marfan Syndrome and Ehlers-Danlos Syndrome | Abnormalities, Multiple, Bone Diseases, Developmental, Cardiovascular Abnormalities, Collagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Ehlers-Danlos syndrome, Hemic and Lymphatic Diseases, Marfan syndrome, Skin Abnormalities, Skin and Connective Tissue Diseases, bone disorder, cardiovascular disorder, congenital heart disease, connective tissue disorder, heart disorder, hematologic disorder, hemorrhagic disease, hereditary disease, hereditary skin disorder, musculoskeletal system disorder, skin disorder, vascular disorder, vascular hemostatic disease | Not yet recruiting | Not stated | 2025-09-12 | NCT07169669 | |
| Analysis of Muscular Properties in Patients With MFS and EDS | Abnormalities, Multiple, Bone Diseases, Developmental, Cardiovascular Abnormalities, Collagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Ehlers-Danlos syndrome, Fatigue, Hemic and Lymphatic Diseases, Marfan syndrome, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Rare Diseases, Signs and Symptoms, Skin Abnormalities, Skin and Connective Tissue Diseases, bone disorder, cardiovascular disorder, congenital heart disease, connective tissue disorder, heart disorder, hematologic disorder, hemorrhagic disease, hereditary disease, hereditary skin disorder, musculoskeletal system disorder, skin disorder, vascular disorder, vascular hemostatic disease | Active, not recruiting | Not stated | 2025-09-10 | NCT05720923 | |
| Marfan Syndrome (MFS) and Facial Dysmorphism: Non-invasive 3D Assessment | Abnormalities, Multiple, Bone Diseases, Developmental, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Marfan syndrome, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Rare Diseases, Skin and Connective Tissue Diseases, bone disorder, cardiovascular disorder, congenital heart disease, connective tissue disorder, heart disorder, hereditary disease, musculoskeletal system disorder | Recruiting | Not stated | 2025-01-13 | NCT05702476 | |
| Marfan Syndrome Moderate Exercise Trial II | Abnormalities, Multiple, Bone Diseases, Developmental, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Marfan syndrome, Skin and Connective Tissue Diseases, bone disorder, cardiovascular disorder, congenital heart disease, connective tissue disorder, heart disorder, hereditary disease, musculoskeletal system disorder | Recruiting | Not applicable | 2024-01-24 | NCT05809323 |