common.study.topics.clinical

Immediate Postpartum Contraceptive Intrauterine Devices

common.study.values.description

Immediate Postpartum Insertion of Contraceptive Intrauterine Devices

In this randomized trial, investigators intend to determine the expulsion and discontinuation rate of immediate postpartum intrauterine devices in the patient population of the University of Oklahoma Women's Healthcare Specialists Clinic (OUWHSC).

common.study.values.location

participant.ui.study.affiliations-map.online-study.header-virtual

participant.ui.study.affiliations-map.online-study.text

participant.ui.study.affiliations-map.legend.locations participant.ui.study.affiliations-map.legend.selected

common.study.values.methods

Pharmaceutical medication involved common.study.methods.has-drugs-yes
Patients and healthy individuals accepted common.study.methods.is-healthy-no

Drug - Skyla Intrauterine System

Participant will be randomly allocated to this intervention

Drug - Mirena Intrauterine System

Participant will be randomly allocated to this intervention

participant.views.study.view.additional

participant.views.study.view.scientific-title

Immediate Postpartum Insertion of Skyla vs Mirena Contraceptive Intrauterine Devices

common.study.values.clinical-trial-id

NCT03657602

participant.views.study.view.id

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