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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Molecular Studies on Hereditary Haemorrhagic Telangiectasia FamiliesCardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, cardiovascular disorder, hematologic disorder, hemorrhagic disease, hereditary hemorrhagic telangiectasia, telangiectasis, vascular disorder, vascular hemostatic disease, vascular malformationRecruitingNot stated2023-09-28NCT00230620

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Research sitesCityCountryLinked trials
Imperial College Hammersmith CampusLondonUnited Kingdom2