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NCT00669396 · ClinicalTrials.gov registry record · NA
Copper T380 IUD Versus Oral Levonorgestrel for Emergency Contraception vs. Plan B for Emergency Contraception
A NA study, sponsored by University of Utah.
- Completed
- Registry status
- NA
- Development phase
- 57
- Enrollment target
NCT00669396 is a NA study that has completed, run by University of Utah. The registered enrollment target is 57 participants.
The verdict
NCT00669396, a NA study, has completed, sponsored by University of Utah.
- COMPLETED
- Registry status
- NA
- Development phase
- 57 participants
- Enrollment target
Study Summary
The purpose of this study is to see if women presenting for emergency contraception (EC) are willing to accept the copper intrauterine device (IUD). This study will also compare the use of effective methods of contraception between women who selected the copper IUD or Plan B 6 months after they received EC.
Interventions
- DRUG levonorgestrel
- DRUG Copper T380 IUD
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 57 participants |
| Start Date | 2008-04 |
| Est. Completion | 2009-05 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00669396
The ClinicalTrials.gov registry entry for NCT00669396 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 57 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 levonorgestrel is the first listed.
NCT00669396 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00669396 about?
NCT00669396 is a clinical study titled "Copper T380 IUD Versus Oral Levonorgestrel for Emergency Contraception vs. Plan B for Emergency Contraception". The purpose of this study is to see if women presenting for emergency contraception (EC) are willing to accept the copper intrauterine device (IUD). This study will also compare the use of effective methods of contraception between women who selected the copper IUD or Plan B 6 months after they rece...
What is the current status of trial NCT00669396?
This trial is currently completed. It is a NA study. The enrollment target is 57 participants. The study started on 2008-04. Estimated completion is 2009-05.
What interventions are being tested in trial NCT00669396?
The interventions under investigation include: levonorgestrel (DRUG), Copper T380 IUD (DRUG).
Who is sponsoring clinical trial NCT00669396?
This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.
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