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Genotype and Phenotype Correlation in Hereditary Thrombotic Thrombocytopenic Purpura (Upshaw-Schulman Syndrome)

Genotype and Phenotype Correlation in Hereditary Thrombotic Thrombocytopenic Purpura (Upshaw-Schulman Syndrome)

Recruiting · NCT01257269 · Registry updated 2023-10-11
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Clinical trials

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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Genotype and Phenotype Correlation in Hereditary Thrombotic Thrombocytopenic Purpura (Upshaw-Schulman Syndrome)Cytopenia, Familial Thrombotic Thrombocytopenic Purpura, Hemic and Lymphatic Diseases, Hemorrhage, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Skin Manifestations, anemia, blood coagulation disease, blood platelet disease, congenital thrombotic thrombocytopenic purpura, hematologic disorder, hemolytic anemia, purpura, thrombocytopenia, thrombocytopenic purpura, thrombophilia, thrombotic microangiopathy, thrombotic thrombocytopenic purpuraRecruitingNot stated2023-10-11NCT01257269

4 results · Page 1 of 1

7 results · Page 1 of 1

Research sites

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Research sitesCityCountryLinked trials
Institute of Hematology and Blood Transfusion, Coagulation Laboratory, U nemocnice 1PragueCzechia1
Medical University of Vienna, Department of Medicine 1, Div. Hematology and Hemostasis Waehringer Guertel 18-20ViennaAustria1
Nara Medical University, Department of Blood Transfusion Medicine, Shijyo-cho 840KashiharaJapan1
Trondheim University St Olavs Hospital, Department of Hematology, PO Box 3250 SluppenTrondheimNorway1
University Clinic of Hematology and Central Hematology Laboratory, Bern University Hospital and the University of Bern, InselspitalBernSwitzerland1
University Medical Center Hamburg-Eppendorf, Department of Pediatric Hematology and Oncology, Martinistr 52HamburgGermany1
University of Oklahoma Health Sciences Center, Department of Medicine, PO Box 26901Oklahoma CityUnited States1