Purpose of this Study
A registry is a database of information (data) about patients living with a specific condition. Scientists study the information in the registry to increase what we know about the condition so we can develop better treatments in the future.
We have created this registry to collect and store medical data, blood and urine samples from people with an autoimmune disease or rheumatic conditions during pregnancy for possible use in future research.
We have created this registry to collect and store medical data, blood and urine samples from people with an autoimmune disease or rheumatic conditions during pregnancy for possible use in future research.
Who Can Participate?
Eligibility
Adult women who are pregnant and have an autoimmune disease or a rheumatic condition.
Sex/Genders
Female (cisgender)
Non-binary or gender fluid
Transgender male
Looking for Healthy Participants
No
What is Involved?
If you choose to join this registry, you will:
- Fill out questionnaires about your health, medical history and quality of life
- Have blood and urine tests
- Give us information about your children to improve our understanding of the effect of autoimmune diseases on babies during and after pregnancy
- Fill out questionnaires about your health, medical history and quality of life
- Have blood and urine tests
- Give us information about your children to improve our understanding of the effect of autoimmune diseases on babies during and after pregnancy
Locations
Duke University Hospital
Visit Timing
Weekdays
Compensation
No
Spanish Materials Available
No
Study Details
Full Title
Maternal Autoimmune Disease Research Alliance (MADRA) Registry
Principal Investigator
Megan
Clowse
Protocol Number
PRO00084014
NCT ID
NCT03276923
Phase
N/A
Enrollment Status
OPEN TO ACCRUAL