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Clinical Trial Summary

An observational cohort study on safety and efficacy of the 220 mg dose Pradaxa to generate additional data in predefined sub populations of patients at increased risk of bleeding or VTE


Clinical Trial Description

n/a


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT00846807
Study type Observational
Source Boehringer Ingelheim
Contact
Status Completed
Phase N/A
Start date February 2009

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