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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01592058
Acronym
BMI
Enrollment
427
Registered
2012-05-04
Start date
2010-06-30
Completion date
2012-05-31
Last updated
2012-07-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Weight Change

Keywords

weight change, contraception, birth control, progestin, progestin only, weight gain, depo, Depo Provera, DMPA, IUD, IUC, Mirena, Paragard, Implanon, implant

Brief 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.

Interventions

None listed

Sponsors

Washington University School of Medicine
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients enrolled in CHOICE between the ages of 18 and 45 who consented to future studies * Chose levonorgestrel-releasing IUD, copper IUD, the implant, or DMPA as their CHOICE baseline method * Has baseline height and weight data collected from the on-campus enrollment site * Able to come back to the on-campus enrollment site for consent process and enrollment activities

Exclusion criteria

* Recent history of DMPA use before starting their baseline CHOICE method * Used current method for less than 11 months or more than 12 months and three weeks

Design outcomes

Primary

MeasureTime frameDescription
WeightBaseline and 12 monthsChange in weight from baseline at 12 months.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026