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

University of Kentucky

Status: Withdrawn

Conditions: Intrauterine Device Placement

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT00986089

08-0938-F6A

Details and patient eligibility

About

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.

Sex: Female

Ages: 18 to 40 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Desire an IUD post-partum and are willing to use the copper IUD.
• They will also need to be patients at one of our OBGYN clinics at the university of Kentucky.

Exclusion criteria

• Post-partum hemorrhage,
• Chorioamnionitis (or a fever >101 at the time of cesarean),
• Women on antibiotic or immunosuppressive therapies,
• Cervical dilation > 5 cm at the time of c-section, OR
• Excessive intraoperative blood loss.
• Also women with contraindications to a copper IUD: Wilson's disease, unusual uterine shape or known uterine anomaly.

Trial design

0 participants in 1 patient group

women who have an IUD placed at the time of c-section