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

Status Completed

Clinical Trial Summary

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.

Clinical Trial Description

Women will be enrolled in this study during late prenatal care. Consent for placement of the IUD will be verified prior to elective C-section. After removal of the placenta, the copper IUD will be placed through the incision at the fundus and the tail strings will be delivered through the cervix. Data will be collected about patient bleeding and possible infection during the immediate postoperative period. The visibility of the strings will be verified at discharge and at 2 and 6 weeks postpartum. Fundal placement of the IUD will be verified by ultrasound at the patient's last visit. ;

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Contraception

Clinical Trial Details

NCT number	NCT00733278
Study type	Interventional
Source	Los Angeles Biomedical Research Institute
Contact
Status	Completed
Phase	Phase 4
Start date	November 2007
Completion date	September 2008

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