MADRA Registry (Women with Autoimmune & Rheumatologic Diseases)

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.

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?

Description

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

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 Enrollment