Clinical Trials Directory

Trials / Completed

CompletedNCT01592058

Weight Change Among Users of Three Progestin-Only Methods of Contraception Over a 12-Month Time Period

Status
Completed
Phase
Study type
Observational
Enrollment
427 (actual)
Sponsor
Washington University School of Medicine · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to learn whether women who use progestin-only methods of birth control such as the contraceptive implant (Implanon), the levonorgestral-releasing IUS (Mirena), or depot medroxyprogesterone acetate(DMPA) will experience weight change compared to women using the non-hormonal copper IUC (ParaGard). The investigators primary hypothesis is that users of DMPA will gain excess weight and increase their BMI above the copper-IUC users; secondarily, the investigators will compare users' data in the LNG-IUC and ENG implant groups to the copper-IUC group.

Conditions

Timeline

Start date
2010-06-01
Primary completion
2012-05-01
Completion
2012-05-01
First posted
2012-05-04
Last updated
2012-07-31

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01592058. Inclusion in this directory is not an endorsement.