Clinical Trials Directory

Trials / Completed

CompletedNCT03064412

Effect of Pregnancy on Androgenic Steroids in Different Genetic Panels

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
70 (actual)
Sponsor
Unity Health Toronto · Academic / Other
Sex
Female
Age
18 Years – 40 Years
Healthy volunteers
Accepted

Summary

Androgens are important sex steroids in women. Androgens influence protein synthesis and muscle growth, are involved in maturation of the reproductive organs, have a fat reducing effect , have a negative effect on the serum lipid profile, and may also increase insulin resistance and coagulation activity. The role of androgens in women is not clear. This study is aimed at learning about the amount of androgen and its actions in pregnant women. This study is also looking to see if there are specific patient factors (such as genetics) that change the amount of androgen and its activity.

Detailed description

There is a lot of information about the main female sex hormones such as estrogens and progesterones (the main female sex hormones and the most important in menstrual , reproductive cycles and pregnancy) . However there is little information about androgens in pregnant women. It is known that certain illnesses, chemicals and dietary products might change the amount of androgen and its actions, which could affect the mother and her baby. It is also known that there are differences between the androgen levels in different people, and in different ethnic groups. These differences are mostly due to genetic factors. The goal of this study is to learn about the androgen levels in healthy pregnant women and if genetic or clinical factors (for example age, trimester of pregnancy, parity, ethnicity, etc.) play a role in changing the androgen amount and action, throughout pregnancy and after delivery.

Conditions

Interventions

TypeNameDescription
BIOLOGICALUrine sample collectionA urine sample will be collected in each of the 3 trimesters of pregnancy, and also at 6 weeks post partum.
BIOLOGICALSaliva collectionA saliva sample will be collected at one time point during the study - likely at the initial baseline visit.

Timeline

Start date
2014-09-01
Primary completion
2017-01-01
Completion
2017-01-01
First posted
2017-02-27
Last updated
2017-07-24

Source: ClinicalTrials.gov record NCT03064412. Inclusion in this directory is not an endorsement.