Immediate Postplacental Insertion of IUDs at Time of Cesarean Delivery: A Randomized Clinical Trial

Completed · Not applicable

Conditions studied: Intrauterine Devices, Cesarean Section

In brief

This is a randomized controlled trial among women who deliver by cesarean at UNC Women's Hospital and desire an Intrauterine Device (IUD) for contraception postpartum. After consenting, women will be randomized to receive an IUD at time of cesarean delivery or at a postpartum visit 4-8 weeks later. After randomization, subjects will be given a choice of the Mirena® IUD or the Paragard® IUD. Data collection will occur at baseline, delivery, the 4-8 week postpartum visit, and 2 follow-up encounters at 3 and 6 months. We hypothesize that women who receive an IUD at the time of cesarean will be more likely to use an IUD 6 months later than women who plan on receiving an IUD 4-8 weeks after delivery.

Key facts

Study ID

NCT01539759

Run by

University of North Carolina, Chapel Hill

People needed

112

Starts

2012-03-01

Expected to finish

2014-08-01

Last updated by the study team

2017-10-13

Who can join

Age: 18 and older, up to 45. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Women ages 18-45
• Pregnant and greater than or equal to 24 weeks of estimated gestational age
• Live Pregnancy
• States a plan to use an Intrauterine Device (IUD) postpartum for contraception
• Plan for cesarean delivery
• Intend to stay in the Chapel Hill area for at least 6 months after birth
• Fluent in English or Spanish

You may not qualify if…

• known uterine anomalies
• allergies to any component of the IUD of their choosing
• known or suspected carcinoma of the breast
• known acute liver disease or liver tumor (benign or malignant)
• known or suspected uterine or cervical neoplasia
• active pelvic inflammatory disease
• genital bleeding of unknown etiology
• history of solid organ transplantation
• positive test for gonorrhea or chlamydia during this pregnancy

Where it is running

• University of North Carolina, Chapel Hill — Chapel Hill, North Carolina, United States

Full record on ClinicalTrials.gov

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