Primovist Post-marketing Surveillance in Japan

Clinical Trial Summary

This study is a regulatory post marketing surveillance in Japan, and it is a local prospective and observational study of patients who have received Primovist for contrast enhancement in MRI of liver. The objective of this study is to assess safety, especially in relation to renal dysfunction, and efficacy of using Primovist in clinical practice. A total 2,000 patients for diagnosis on detection and identify hepatic tumor will be recruited and followed 7 days after the injection.

See also
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NCT number	NCT01411449
Study type	Observational
Source	Bayer
Contact
Status	Completed
Phase	N/A
Start date	March 11, 2008
Completion date	February 18, 2015

Primovist Post-marketing Surveillance in Japan — PRIMOVIST

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms