Intrauterine Contraceptive Device (IUD) Placement at Time of C-Section

Completed · Phase 4

Conditions studied: Contraception

In brief

This is a pilot study of up to 10 women, which will test the hypothesis that the placement of copper IUDs through the uterine incision at the time of uncomplicated elective C-section is technically feasible and acceptable to women seeking long-term contraception.

Key facts

Study ID

NCT00733278

Run by

Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center

People needed

7

Starts

2007-11-01

Expected to finish

2008-09-01

Last updated by the study team

2014-08-11

Who can join

Age: 18 and older, up to 50. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Pregnant woman
• Requires elective C-section
• Desires long-term contraception

You may not qualify if…

• Contraindications to copper IUD

Where it is running

• Los Angeles BRI — Torrance, California, United States

Full record on ClinicalTrials.gov

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