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Clinical Trial Summary

The purpose of this study is to prospectively obtain reliable data on the bleeding and treatment pattern of patients with VWD undergoing on-demand treatment with a VWF-containing product over a period of 6 months. The data obtained will be used as a basis for historical comparisons with the bleeding and treatment pattern obtained from a clinical study on the efficacy of prophylactic treatment with a VWF/FVIII concentrate.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04053699
Study type Observational
Source Octapharma
Contact
Status Completed
Phase
Start date June 25, 2019
Completion date January 31, 2021

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