Mirena Post-marketing Surveillance in Japan

Status Completed

Clinical Trial Summary

This study is a regulatory post-marketing surveillance in Japan, and it is a local prospective and observational study of women who are inserted Mirena for intrauterine contraception. The objective of this study is to assess safety and effectiveness of Mirena under real-life practice conditions. A total 550 patients will be recruited and followed for 5 years.

Clinical Trial Description

n/a

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

Contraception

Clinical Trial Details

NCT number	NCT01414140
Study type	Observational
Source	Bayer
Contact
Status	Completed
Phase	N/A
Start date	May 2007
Completion date	October 2012

View Details

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