The Preeclampsia Registry
Recruiting now
Conditions studied: Preeclampsia, Eclampsia, HELLP Syndrome, Toxemia, Hypertensive Disorder of Pregnancy
In brief
The purpose of The Preeclampsia Registry is to collect and store medical and other information from women who have been medically diagnosed with preeclampsia or a related hypertensive (high blood pressure) disorder of pregnancy such as eclampsia or HELLP syndrome, their family members, and women who have not had preeclampsia to serve as controls. Information from participants will be used for medical research to try to understand why preeclampsia occurs, how to predict it better, and to develop experimental clinical trials of new treatments. The Registry will consist of a web-based survey and mechanism for collecting and reviewing medical records. This data will be utilized for immediate investigator-driven cross-sectional research projects (after proposal review by the Registry's scientific advisory board and as directed by the PI). Participants may also choose to be contacted regarding possible participation in future studies, about providing a biospecimen, as well as investigator-driven clinical trials. The Registry is anticipated to exist long-term and to serve as a foundation of participants from which to draw for studies of preeclampsia, anticipated to evolve as our scientific understanding of preeclampsia evolves.
Key facts
- Study ID
- NCT06377878
- Run by
- Preeclampsia Foundation
- People needed
- 20000
- Starts
- 2013-09-01
- Expected to finish
- 2040-05-01
- Last updated by the study team
- 2024-04-22
Who can join
Age: 13 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Women who were medically diagnosed with preeclampsia or a related hypertensive disorder of pregnancy (HDP) such as eclampsia or HELLP syndrome.
- Female or Male relatives of affected women
- Women who have never had preeclampsia or hypertensive disorders of pregnancy, but who would like to serve as "controls" in research studies of preeclampsia.
- An authorized representative may complete the questionnaire and provide consent for a woman who had preeclampsia, but has died or is disabled as a result.
You may not qualify if…
- Those unable to provide consent
- Prisoners
- Individuals unable to speak English
Where it is running
- Preeclampsia Foundation — Melbourne, Florida, United States (enrolling)
Full record on ClinicalTrials.gov
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