Patient Compliance With Long-Acting Reversible Contraception Administration

Stopped early · Not applicable

Conditions studied: Contraception

In brief

This a randomized control trial to identify if patients who desire LARC are more likely to have success receiving the desired form of contraception if it is placed a) during the postpartum hospital stay, either in the immediate or early postpartum period, versus b) during the interval postpartum period as previously done.

Key facts

Study ID

NCT03305081

Run by

Tulane University School of Medicine

People needed

45

Starts

2014-10-22

Expected to finish

2016-05-31

Last updated by the study team

2021-01-22

Who can join

Age: 15 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Pregnant, desires LARC postpartum

You may not qualify if…

• Medical contraindication to desired LARC, vaginal delivery complicated by fourth degree perineal laceration, history of pelvic inflammatory disease, uterine infection

Where it is running

• Tulane Department of Obstetrics and Gynecology — New Orleans, Louisiana, United States

Full record on ClinicalTrials.gov

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