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Clinical Trial Summary

This open-label, prospective, multi-center, non-interventional, observational, parallel cohort study intended to provide real life data on the treatment duration, effectiveness and safety of tedizolid and linezolid when treating ABSSSI hospitalized patients in a real practice setting.


Clinical Trial Description

The primary objective of this study was to assess the treatment duration in the real life in 2 cohorts consisting of patients treated by 200 mg once daily IV/PO tedizolid or treated by 600 mg twice daily IV/PO (intravenous/per oral) linezolid. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02991131
Study type Observational
Source Bayer
Contact
Status Terminated
Phase
Start date December 17, 2016
Completion date November 21, 2018

See also
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