Participate In Research
Participate In Research
Patients like you are central to moving preeclampsia research forward.
Although we now understand more about what causes preeclampsia, there are still so many unanswered questions that your experience can help us understand:
Why does preeclampsia happen in some pregnancies and not others?
Why does preeclampsia happen to some women who have no risk factors?
Why is preeclampsia more severe in some patients?
How does preeclampsia affect women beyond their pregnancy experiences, including their long-term physical and mental well-being?
All of these questions and more are being studied by researchers around the world and right here, thanks in no small part to the Preeclampsia Foundation community and our continued drive to fund and support research on preeclampsia, HELLP syndrome, and related hypertensive disorders of pregnancy.
As a patient, the choice to participate in any research study is up to you. Here’s how YOU can get involved.
The Preeclampsia Registry is a secure research database that brings your pregnancy experience(s), medical information and even your DNA, if you wish, together with leading researchers to make preeclampsia a disease of the past.
As a participant, you will join thousands of other women and families in supporting several research studies to accelerate the discoveries of the causes of preeclampsia and better options for prevention, diagnosis, and treatment.
Your experiences help researchers at every stage of the research process: from study design, to recruitment, to driving participation, and even sharing results.
The Preeclampsia Foundation Canada is regularly invited to provide your patient perspective as members of our community. For more information about patients as research partners and other ways to participate in research, please contact us.