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NCT01990703 · ClinicalTrials.gov registry record · Phase 4
BLIS - Breastfeeding Levonorgestrel IUD Study
A Phase 4 study, sponsored by University of Utah.
- Completed
- Registry status
- Phase 4
- Development phase
- 285
- Enrollment target
NCT01990703 is a Phase 4 study that has completed, run by University of Utah. The registered enrollment target is 285 participants.
The verdict
NCT01990703, a Phase 4 study, has completed, sponsored by University of Utah.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 285 participants
- Enrollment target
Study Summary
We are studying the effect of placing the levonorgestrel IUD (Mirena) immediately after birth on breastfeeding. Women who wish to have a levonorgestrel IUD placed after their birth, wish to breastfeed, and are willing to participate in the study will be randomly assigned to either get the IUD placed immediately after delivery of the baby and placenta or 4-6 weeks later. We do not believe there will be a difference in breastfeeding 8 weeks after delivery between those who get the IUD placed early or later.
Interventions
- DRUG Levonorgestrel IUD
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 285 participants |
| Start Date | 2014-01 |
| Est. Completion | 2017-01 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01990703
The ClinicalTrials.gov registry entry for NCT01990703 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 285 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 1 intervention - of which Levonorgestrel IUD is the first listed.
NCT01990703 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01990703 about?
NCT01990703 is a clinical study titled "BLIS - Breastfeeding Levonorgestrel IUD Study". We are studying the effect of placing the levonorgestrel IUD (Mirena) immediately after birth on breastfeeding. Women who wish to have a levonorgestrel IUD placed after their birth, wish to breastfeed, and are willing to participate in the study will be randomly assigned to either get the IUD placed...
What is the current status of trial NCT01990703?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 285 participants. The study started on 2014-01. Estimated completion is 2017-01.
What interventions are being tested in trial NCT01990703?
The interventions under investigation include: Levonorgestrel IUD (DRUG).
Who is sponsoring clinical trial NCT01990703?
This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.
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