Ehlers-Danlos syndrome, vascular type
Ehlers-Danlos syndrome, vascular type
Explore linked clinical trials. Standard reference: MONDO:00173148 results · Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| 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 | |
| An Exercise and Lifestyle Programme for Adults With Vascular Ehlers-Danlos Syndrome: A Feasibility Study | Aneurysm, Aortic Dissection, Collagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Dissection, Blood Vessel, Ehlers-Danlos syndrome, Ehlers-Danlos syndrome, vascular type, Hemic and Lymphatic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Rare Diseases, Skin Abnormalities, Skin and Connective Tissue Diseases, cardiovascular disorder, connective tissue disorder, hematologic disorder, hemorrhagic disease, hereditary disease, hereditary skin disorder, skin disorder, vascular disorder, vascular hemostatic disease | Not yet recruiting | Not applicable | 2026-07-13 | NCT07697573 | |
| 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 | |
| Metabolic Phenotyping in vEDS | Aneurysm, Aortic Dissection, Collagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dissection, Blood Vessel, Ehlers-Danlos syndrome, Ehlers-Danlos syndrome, vascular type, Hemic and Lymphatic Diseases, Insulin Resistance, Nutritional and Metabolic Diseases, Skin Abnormalities, Skin and Connective Tissue Diseases, acquired partial lipodystrophy, cardiovascular disorder, connective tissue disorder, glucose metabolism disease, hematologic disorder, hemorrhagic disease, hereditary disease, hereditary skin disorder, hyperinsulinism, metabolic disease, skin disorder, vascular disorder, vascular hemostatic disease | Recruiting | Not stated | 2026-04-08 | NCT07516496 | |
| 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 | |
| SEDVasc (RaDiCo Cohort) (RaDiCo-SEDVasc) | Aneurysm, Aortic Dissection, Collagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dissection, Blood Vessel, Ehlers-Danlos syndrome, Ehlers-Danlos syndrome, vascular type, Hemic and Lymphatic Diseases, Skin Abnormalities, Skin and Connective Tissue Diseases, cardiovascular disorder, connective tissue disorder, hematologic disorder, hemorrhagic disease, hereditary disease, hereditary skin disorder, skin disorder, vascular disorder, vascular hemostatic disease | Active, not recruiting | Not stated | 2026-02-12 | NCT05976841 | |
| Clinical Trial to Compare the Efficacy of Celiprolol to Placebo in Patients With Vascular Ehlers-Danlos Syndrome | Aneurysm, Aortic Dissection, Collagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dissection, Blood Vessel, Ehlers-Danlos syndrome, Ehlers-Danlos syndrome, vascular type, Hemic and Lymphatic Diseases, Skin Abnormalities, Skin and Connective Tissue Diseases, cardiovascular disorder, connective tissue disorder, hematologic disorder, hemorrhagic disease, hereditary disease, hereditary skin disorder, skin disorder, vascular disorder, vascular hemostatic disease | Recruiting | Phase 3 | 2025-08-24 | NCT05432466 | |
| Heart Coherence Training on Vascular Ehlers-Danlos Syndrome Patients | Aneurysm, Aortic Dissection, Collagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dissection, Blood Vessel, Ehlers-Danlos syndrome, Ehlers-Danlos syndrome, vascular type, Hemic and Lymphatic Diseases, Skin Abnormalities, Skin and Connective Tissue Diseases, cardiovascular disorder, connective tissue disorder, hematologic disorder, hemorrhagic disease, hereditary disease, hereditary skin disorder, skin disorder, vascular disorder, vascular hemostatic disease | Recruiting | Not applicable | 2024-07-01 | NCT05994664 |