CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 63,194 enrolled
Drug / intervention
Not specified
Likely dose
Not stated in record
Key inclusion· 2
  • ✓New insertion of an IUD
  • ✓Willing to participate in cohort study
Key exclusion· 2
  • ✕Not cooperative
  • ✕Language barrier

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00461175
NCT00461175N/ACompleted
CompareCT.gov

European Active Surveillance Study for Intrauterine Devices

Center for Epidemiology and Health Research, Germany·observational·Posted Apr 17, 2007·Updated Jul 17, 2015

In Brief

An observational study for Uterine Perforation. Completed, enrolled 63,194 participants across 1 site.

Detailed 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 clinical outcome of interest is the uterine perforation rate.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsUterine Perforation
CountriesGermany
CollaboratorsBayer

Timeline

N/ACompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedApr 17, 2007
Enrollment StartNov 1, 2006
Primary CompletionMay 1, 2012
Study CompletionDec 1, 2013
TodayJul 2, 2026
Enrollment to primary: 5.5 yearsPosted 19.2 years ago