Status:
COMPLETED
European Active Surveillance Study for Intrauterine Devices
Lead Sponsor:
Center for Epidemiology and Health Research, Germany
Collaborating Sponsors:
Bayer
Conditions:
Uterine Perforation
Eligibility:
FEMALE
18+ years
Brief Summary
The primary objective of the study is to assess the risks of intrauterine device (IUD) use in a study population that is representative for the actual users of the individual IUDs. The primary clinica...
Detailed Description
This is a large, multinational, prospective, controlled, long-term cohort study that follows a series of cohorts. The cohorts consist of new users of different groups of intrauterine devices (IUDs). P...
Eligibility Criteria
Inclusion
- women who have a new insertion of an IUD
- women who are willing to participate in this cohort study
Exclusion
- women who are not cooperative
- women with a language barrier
Key Trial Info
Start Date :
November 1 2006
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
December 1 2013
Estimated Enrollment :
63194 Patients enrolled
Trial Details
Trial ID
NCT00461175
Start Date
November 1 2006
End Date
December 1 2013
Last Update
July 17 2015
Active Locations (1)
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1
Center for Epidemiology and Health Research
Berlin, Germany, 10115