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Trial record 1 of 1 for:    NCT01257269
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Genotype and Phenotype Correlation in Hereditary Thrombotic Thrombocytopenic Purpura (Upshaw-Schulman Syndrome) (TTP registry)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT01257269
Recruitment Status : Recruiting
First Posted : December 9, 2010
Last Update Posted : November 18, 2020
Swiss National Science Foundation
Mach Gaensslen Foundation
Baxalta Innovations GmbH, Wien, Austria
Information provided by (Responsible Party):
University Hospital Inselspital, Berne

No Study Results Posted on for this Study
Recruitment Status : Recruiting
Estimated Primary Completion Date : October 2030
Estimated Study Completion Date : October 2030
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