Klippel-Trenaunay-Weber Syndrome: 24 Clinical Trials, Page 3 of 3

Vascular Anomaly Pathology and Genomics Biopsy Study

Condition(s):Vascular Malformations; Vascular Anomaly; Hemangioma; Arteriovenous Malformations; Venous Malformation; Klippel Trenaunay Syndrome; Lymphatic MalformationLast Updated:April 21, 2022Completed

Lymphatic Anomalies Registry for the Assessment of Outcome Data

Condition(s):Lymphatic Malformation; Generalized Lymphatic Anomaly (GLA); Central Conducting Lymphatic Anomaly; CLOVES Syndrome; Gorham-Stout Disease (“Disappearing Bone Disease”); Blue Rubber Bleb Nevus Syndrome; Kaposiform Lymphangiomatosis; Kaposiform Hemangioendothelioma/Tufted Angioma; Klippel-Trenaunay Syndrome; LymphangiomatosisLast Updated:September 13, 2022Recruiting

Institutional Registry of Haemorrhagic Hereditary Telangiectasia

Condition(s):Haemorrhagic Hereditary TelangiectasiaLast Updated:December 17, 2015Unknown status

Tranexamic Acid and Epistaxis in Hereditary Hemorrhagic Telangiectasia (HHT)

Condition(s):Hereditary Hemorrhagic TelangiectasiaLast Updated:December 15, 2009Completed

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