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Stress Hormones and IUDs

Contraception Clinical Trial

Official title:
Effect of Initiation of Intrauterine Contraception on Hair Cortisol Concentration

Clinical Trial Summary

Determine what kind of side effects women experience in the first year after they start using an intrauterine device.

Clinical Trial Description

The purpose of this study is to find out if there is a difference in levels of stress hormones in women who use copper or hormonal intrauterine devices (IUDs). This study will provide more information on the potential effect of levonorgestrel intrauterine system (LNG-IUS) use on an individual's stress response. Ultimately, this study hopes to provide data to better counsel women on potential mood effects of the LNG-IUS. From a research and clinical management perspective, hair cortisol may provide a tool to evaluate women at risk for discontinuation of hormonal contraception due to concern of mood symptoms. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03499379
Study type Observational
Source Oregon Health and Science University
Contact
Status Completed
Phase
Start date April 16, 2018
Completion date December 31, 2019
View Details
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