The Preeclampsia Registry is collecting health information from women who have had preeclampsia or related high blood pressure disorders during pregnancy (like eclampsia or HELLP syndrome), their family members, and women who have never had these conditions. This information will be used for medical research to better understand why preeclampsia happens, how to predict it, and to help develop new treatments. You would share your medical history and other details through a web-based survey, and your medical records would be reviewed. The goal is to gather enough information to improve care for mothers and babies affected by preeclampsia. The study aims to enroll 20,000 participants and is currently unclear on its status.

Study design

This is an observational study aiming to enroll 20,000 participants. It is not testing a specific intervention.

What's involved

You would complete a web-based survey and allow for the collection and review of your medical records. This information will be assessed yearly, for up to 20 years.

Compensation

Not stated in the trial record.

Follow-up

Your self-reported diagnosis of preeclampsia and hypertensive disorders of pregnancy, confirmed by medical records, will be assessed yearly, up to 20 years.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.