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NCT02175030 · ClinicalTrials.gov registry record · Phase 4
RAPID EC - Rct Assessing Pregnancy With Intrauterine Devices for EC
A Phase 4 study, sponsored by University of Utah.
- Completed
- Registry status
- Phase 4
- Development phase
- 711
- Enrollment target
NCT02175030 is a Phase 4 study that has completed, run by University of Utah. The registered enrollment target is 711 participants.
The verdict
NCT02175030, a Phase 4 study, has completed, sponsored by University of Utah.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 711 participants
- Enrollment target
Study 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.
Interventions
- DRUG Copper IUD
- DRUG Levonorgestrel IUD
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 711 participants |
| Start Date | 2016-08 |
| Est. Completion | 2020-12 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02175030
The ClinicalTrials.gov registry entry for NCT02175030 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 711 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Utah, which has 818 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Copper IUD is the first listed.
NCT02175030 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02175030 about?
NCT02175030 is a clinical study titled "RAPID EC - Rct Assessing Pregnancy With Intrauterine Devices for EC". 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...
What is the current status of trial NCT02175030?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 711 participants. The study started on 2016-08. Estimated completion is 2020-12.
What interventions are being tested in trial NCT02175030?
The interventions under investigation include: Copper IUD (DRUG), Levonorgestrel IUD (DRUG).
Who is sponsoring clinical trial NCT02175030?
This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.
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