Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT00986089

Intrauterine Device (IUD) Placement at the Time of Cesarean Section

Pilot Study of Copper IUD Placement at the Time of Cesarean Section

Status
Withdrawn
Phase
Study type
Observational
Enrollment
0 (actual)
Sponsor
University of Kentucky · Academic / Other
Sex
Female
Age
18 Years – 40 Years
Healthy volunteers
Accepted

Summary

To evaluate the continuation of the Copper IUD at one year after placement through the cesarean incision into the uterus at the time of cesarean section.

Conditions

Timeline

Start date
2008-08-01
Primary completion
2010-07-01
Completion
2010-07-01
First posted
2009-09-29
Last updated
2016-12-22

Source: ClinicalTrials.gov record NCT00986089. Inclusion in this directory is not an endorsement.