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NCT01963962 · ClinicalTrials.gov registry record
Study of the Copper IUD or Oral Levonorgestrel and the Levonorgestrel IUD for Women Seeking Emergency Contraception
A clinical trial, sponsored by University of Utah.
- Completed
- Registry status
- 188
- Enrollment target
NCT01963962: Completed study, sponsored by University of Utah.
NCT01963962 is a clinical trial that has completed, run by University of Utah. The registered enrollment target is 188 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01963962 has completed, sponsored by University of Utah.
- COMPLETED
- Registry status
- 188 participants
- Enrollment target
Study Summary
The purpose of this study is to see how often women who come to a family planning clinic for emergency contraception, the morning after pill, are willing to use either the copper IUD or the levonorgestrel IUD. The investigators will also see if pregnancies occur in those choosing the levonorgestrel IUD and if people continue to use the IUD for 1 year.
Primary Outcome
Participants will have a urine pregnancy test at the clinic. They will also be given a home urine pregnancy test to check if they are not able to return to clinic and will give results by phone or electronic communication.
Interventions
- DRUG Copper IUD
- DRUG Levonorgestrel IUD
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 188 participants |
| Start Date | 2013-07 |
| Est. Completion | 2016-02 |
What the finished NCT01963962 record still lists
NCT01963962 is an observational study that tracks outcomes without assigning an intervention. The registered 188 participants enrollment target is mid-sized for trials with a published cap.
The record links to 0 conditions, and to 2 interventions - of which Copper IUD is the first listed.
NCT01963962 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01963962 about?
NCT01963962 is a clinical study titled "Study of the Copper IUD or Oral Levonorgestrel and the Levonorgestrel IUD for Women Seeking Emergency Contraception". The purpose of this study is to see how often women who come to a family planning clinic for emergency contraception, the morning after pill, are willing to use either the copper IUD or the levonorgestrel IUD. The investigators will also see if pregnancies occur in those choosing the levonorgestrel ...
What is the current status of trial NCT01963962?
This trial is currently completed. The enrollment target is 188 participants. The study started on 2013-07. Estimated completion is 2016-02.
What interventions are being tested in trial NCT01963962?
The interventions under investigation include: Copper IUD (DRUG), Levonorgestrel IUD (DRUG).
Who is sponsoring clinical trial NCT01963962?
This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.
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