Viewing Study NCT01592058


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Study NCT ID: NCT01592058
Status: COMPLETED
Last Update Posted: 2012-07-31
First Post: 2012-05-02
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Weight Change Among Users of Three Progestin-Only Methods of Contraception Over a 12-Month Time Period
Sponsor: Washington University School of Medicine
Organization:

Study Overview

Official Title: Weight Change Among Users of Three Progestin-Only Methods of Contraception Over a 12-Month Time Period
Status: COMPLETED
Status Verified Date: 2012-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: BMI
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.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: