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CompletedNCT01555931

Postpartum Levonorgestrel-releasing Intrauterine System and Breastfeeding

Immediate vs. 4-8 Week Postpartum Levonorgestrel-releasing Intrauterine System Placement: A Randomized Clinical Trial (Short Title: PPIUD1)

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
61 (actual)
Sponsor
University of North Carolina, Chapel Hill · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

This will be a randomized clinical trial of 190 women aged 18-45 who plan to breastfeed their infant for at least 6 months and desire to use the LNG-IUS as their primary contraceptive method postpartum. The investigators will compare the frequency of breastfeeding among women receiving the levonorgestrel-releasing intrauterine system (LNG-IUS) immediately after vaginal delivery compared to 4-8 weeks later. The investigators hypothesize there will be no difference in breastfeeding prevalence between the two groups.

Conditions

Interventions

TypeNameDescription
DRUGLevonorgestrel-releasing intrauterine systemPlacement within 48 hours of delivery

Timeline

Start date
2012-03-01
Primary completion
2013-06-01
Completion
2013-06-01
First posted
2012-03-16
Last updated
2014-08-25
Results posted
2014-08-25

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01555931. Inclusion in this directory is not an endorsement.

Postpartum Levonorgestrel-releasing Intrauterine System and Breastfeeding (NCT01555931) · Clinical Trials Directory