Trial Condition(s):

Pregnancy

Duration of use of highly effective reversible contraception

Bayer Identifier:

17714

ClinicalTrials.gov Identifier:

NCT02414919

EudraCT Number:

Not Available

Study Completed

Trial Purpose

To assess the proportion of women who use HERC for ≥2 years of duration

Inclusion Criteria
:
-Women who had an IUD or contraceptive implant inserted and removed within the University of Utah from January 1, 2004 to October 31, 2012
Exclusion Criteria
No Exclusion Criteria Available

Trial Summary

Enrollment Goal
13880
Trial Dates
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Phase
N/A
Could I receive a placebo?
No
Products
Mirena (Levonorgestrel IUS, BAY86-5028)
Accepts Healthy Volunteers
No

Where to Participate

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Locations
Status
LocationsStatus
Locations

Investigative Site

Salt Lake, United States

Status
Completed
 

Trial Design