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Clinical Trial Summary

To assess and evaluate the safety of octaplas™ in comparison to standard plasma product (e.g., fresh frozen plasma (FFP) and other approved plasma products used within 24 hours of thawing) used in the treatment of TTP, in patients undergoing Therapeutic Plasma Exchange, with a special emphasis on the occurrence of thromboembolic events (TEEs).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01938404
Study type Observational
Source Octapharma
Contact
Status Terminated
Phase
Start date June 6, 2017
Completion date August 2, 2017

See also
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