Contraception Clinical Trial
Official title:
Immediate Versus Delayed IUD Insertion Following Suction Aspiration Between 5 and 12 Weeks Gestation: a Randomized Trial
The purpose of this multi-center clinical trial is to evaluate the safety and effectiveness
of inserting an intrauterine device (IUD) immediately after a suction aspiration procedure
compared to inserting the IUD 2-6 weeks after the procedure. This study will also evaluate
how satisfied women are with the timing of their IUD placement. Subjects will be able to
choose between the Paraguard IUD or the Mirena IUD.
The researchers hypothesize that:
1. the expulsion rates measured at 1, 3 and 6 months will be clinically equivalent with
immediate insertion compared with delayed insertion,
2. satisfaction and tolerance of side effects will be higher with immediate IUD insertion
compared with delayed insertion, and
3. overall IUD use/continuation rates measured at 1, 3 and 6 months will be higher with
immediate IUD insertion compared with delayed insertion.
n/a
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Prevention
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