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NCT00966771 · ClinicalTrials.gov registry record
The Copper T380A IUD vs. Oral Levonorgestrel for Emergency Contraception
A clinical trial, sponsored by University of Utah.
- Completed
- Registry status
- 548
- Enrollment target
NCT00966771 is a clinical trial that has completed, run by University of Utah. The registered enrollment target is 548 participants.
The verdict
NCT00966771 has completed, sponsored by University of Utah.
- COMPLETED
- Registry status
- 548 participants
- Enrollment target
Study Summary
The purpose of this study is to see if women presenting for emergency contraception (EC) and choose the copper intrauterine device (IUD) will have fewer unplanned pregnancies in the next year compared to women who choose oral levonorgestrel for EC. The study will also compare use of an effective method of contraception in the year after they received EC.
Interventions
- DRUG Copper T380 IUD
- DRUG Oral levonorgestrel
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 548 participants |
| Start Date | 2009-10 |
| Est. Completion | 2011-08 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00966771
The ClinicalTrials.gov registry entry for NCT00966771 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 548 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 T380 IUD is the first listed.
NCT00966771 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00966771 about?
NCT00966771 is a clinical study titled "The Copper T380A IUD vs. Oral Levonorgestrel for Emergency Contraception". The purpose of this study is to see if women presenting for emergency contraception (EC) and choose the copper intrauterine device (IUD) will have fewer unplanned pregnancies in the next year compared to women who choose oral levonorgestrel for EC. The study will also compare use of an effective met...
What is the current status of trial NCT00966771?
This trial is currently completed. The enrollment target is 548 participants. The study started on 2009-10. Estimated completion is 2011-08.
What interventions are being tested in trial NCT00966771?
The interventions under investigation include: Copper T380 IUD (DRUG), Oral levonorgestrel (DRUG).
Who is sponsoring clinical trial NCT00966771?
This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.
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