CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 711 enrolled
Drug / intervention
Copper IUD +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02175030
NCT02175030Phase 4Completed
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RAPID EC - Randomized Controlled Trial Assessing Pregnancy With Intrauterine Devices for Emergency Contraception

University of Utah·interventional·Posted Jun 26, 2014·Updated Jun 29, 2022

In Brief

A Phase 4 clinical trial evaluating Copper IUD and Levonorgestrel IUD for Contraception. Completed, enrolled 711 participants across 6 sites.

Detailed Summary

This study is a randomized trial of two IUDs for emergency contraception: the copper IUD, the most effective method of emergency contraception vs. the levonorgestrel IUD, the most preferred IUD which has never been tested as an emergency contraceptive. This research has the potential to increase use of highly effective contraception in a high-risk population and lower the persistently elevated rate of U.S. unintended pregnancy.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsContraception
CountriesUnited States
Collaborators--

Timeline

Phase 4CompletedFinished
201520162017201820192020202120222023202420252026
First PostedJun 26, 2014
Enrollment StartAug 1, 2016
Primary CompletionFeb 1, 2020
Study CompletionDec 1, 2020
TodayJul 2, 2026
Enrollment to primary: 3.5 yearsPosted 12.0 years ago

Interventions

Copper IUDdrug

Randomization to copper/Paragard IUD for emergency contraception

Levonorgestrel IUDdrug

Randomization to Levonorgestrel/Mirena IUD for emergency contraception