Patient Compliance With Long-Acting Reversible Contraception Administration



Status:Terminated
Conditions:Contraception, Contraception
Therapuetic Areas:Reproductive
Healthy:No
Age Range:15 - Any
Updated:10/11/2017
Start Date:October 22, 2014
End Date:May 31, 2016

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Trial Summary
Trial Overview
Inclusion Criteria

Patient Compliance With Long-Acting Reversible Contraception Administration Immediately and Early Postpartum Versus Interval Postpartum

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.

Randomized control trial with control group receiving LARC at 6 weeks postpartum and the
study group receiving LARC in the immediate or early postpartum period. Outcomes will be
measured by those who receive or do not receive LARC either in the hospital after delivery
versus 6 weeks postpartum in accordance with the study subjects' randomized designation.
Secondary outcomes of bleeding profile and satisfaction will also be assessed.

Inclusion Criteria:

- Pregnant, desires LARC postpartum

Exclusion Criteria:

- Medical contraindication to desired LARC, vaginal delivery complicated by fourth
degree perineal laceration, history of pelvic inflammatory disease, uterine infection
We found this trial at
1
site
Tulane Department of Obstetrics and Gynecology
1542 Tulane Avenue
New Orleans, Louisiana 70018
?
mi
from
New Orleans, LA
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