Clinical Trial

Immediate Postpartum Contraceptive Intrauterine Devices

Study 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).

Location

Locations Selected Location

Methods

Pharmaceutical medication involved Pharmaceutical medication involved
Patients and healthy individuals accepted Patients and healthy individuals accepted

Drug - Skyla Intrauterine System

Participant will be randomly allocated to this intervention

Drug - Mirena Intrauterine System

Participant will be randomly allocated to this intervention

Additional Information

Official Study Title

Immediate Postpartum Insertion of Skyla vs Mirena Contraceptive Intrauterine Devices

Clinical Trial ID

NCT03657602

ParticipAid ID

egJZ3d