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drugset / Trial / NCT03657602

Immediate Postpartum Insertion of Contraceptive Intrauterine Devices

NCT03657602 ↗

Phase 0 Completed 28 enrolled University of Oklahoma
RandomizedParallel-groupSingle-blindOther

Summary

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).

Timeline

Start
2019-12-15
Primary completion
2023-01-15
Completion
2023-01-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Kyleena Intrauterine System Unknown — Other
Subject Mirena Intrauterine System Unknown — Other

Indications

No indication recorded.