Viewing Study NCT01257269


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Study NCT ID: NCT01257269
Status: RECRUITING
Last Update Posted: 2023-10-11
First Post: 2010-12-06
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Genotype and Phenotype Correlation in Hereditary Thrombotic Thrombocytopenic Purpura (Upshaw-Schulman Syndrome)
Sponsor: Insel Gruppe AG, University Hospital Bern
Organization:

Study Modules

Identification Module Status Module Sponsor Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms Interventions Module Outcomes Module Eligibility Module Contacts Locations Module References Module