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Sponsored by: |
University Hospital, Rouen |
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Information provided by: | University Hospital, Rouen |
ClinicalTrials.gov Identifier: | NCT00213473 |
the aims of SACHA study was to appreciate prevalence, evolution and follow-up, treatment response of patients with acquired hemophilia with biological and clinical data. Inclusion criteria were factor VIIIc below 30% associated with presence of Facgteur VIII inhibitor (titer > 1 u Bethesda. Clinical and biologival data were obtained at Day 0 (as soon as possible and at 1, 3, 6 and 12 months.Informations were notified to co-investigators with the help of two french medical society (Internal medicine, french haemostasis and thrombosis society.
Condition |
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Acquired Haemophilia Register |
Study Type: | Observational |
Study Design: | Natural History, Longitudinal, Defined Population, Prospective Study |
Official Title: | Prospective Clinical and Biological Follow-up of Acquired Haemophilia : SACHA Study |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Study ID Numbers: | 2001/001 HP |
Study First Received: | September 13, 2005 |
Last Updated: | June 4, 2007 |
ClinicalTrials.gov Identifier: | NCT00213473 |
Health Authority: | France: Afssaps - French Health Products Safety Agency |
acquired haemophilia |
Hemorrhagic Disorders Genetic Diseases, Inborn Hematologic Diseases |
Blood Coagulation Disorders Hemophilia A Hemostatic Disorders |
Blood Coagulation Disorders, Inherited Coagulation Protein Disorders |