MADRA Registry - Clinical Trial
What is the 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 in the Study?
Adult women who are pregnant and have an autoimmune disease or a rheumatic condition.
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