drugset / Trial / NCT02121067
LNG-IUS at 2 Weeks Postpartum
Phase 4
Completed
50 enrolled
University of North Carolina, Chapel Hill
Society of Family Planning · collab
NaSingle-groupOpen-labelPrevention
Summary
This is a study of 50 postpartum women interested in having the Mirena® LNG-IUS placed for contraception. The Mirena® is an FDA approved intrauterine contraceptive device that provides contraception for 5 years with excellent effectiveness. Women enrolled in this study will only have the Mirena® placed at two-weeks postpartum (day 14-20 postpartum). The participants will be followed at 6-weeks and 6-months postpartum for study visits to evaluate for satisfaction, symptoms, expulsion, and perforation. The study will be completed at six-months postpartum, and participants will be able to keep their LNG-IUS following study completion.
Timeline
- Start
- 2014-09
- Primary completion
- 2016-06
- Completion
- 2016-06
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Levonorgestrel | Small molecule | 52 mg | Other |
Indications
No indication recorded.