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LNG-IUS at 2 Weeks Postpartum — LNG-IUS  

Contraception Clinical Trial

Official title:
Intrauterine Contraceptive Insertion at Two-weeks Postpartum: A Study of Acceptability and Short-term Outcomes

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02121067
Study type Interventional
Source University of North Carolina, Chapel Hill
Contact Matthew L Zerden, MD, MPH
Phone 919-843-5633
Email Matthew_Zerden@med.unc.edu
Status Recruiting
Phase Phase 4
Start date September 2014
Completion date January 2016
View Details
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