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Recruiting NCT06377878

NCT06377878 The Preeclampsia Registry

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Clinical Trial Summary
NCT ID NCT06377878
Status Recruiting
Phase
Sponsor Preeclampsia Foundation
Condition Preeclampsia
Study Type OBSERVATIONAL
Enrollment 20,000 participants
Start Date 2013-09-01
Primary Completion 2040-05

Trial Parameters

Condition Preeclampsia
Sponsor Preeclampsia Foundation
Study Type OBSERVATIONAL
Phase N/A
Enrollment 20,000
Sex ALL
Min Age 13 Years
Max Age N/A
Start Date 2013-09-01
Completion 2040-05

Eligibility Fast-Check

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Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: * 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. Exclusion Criteria: * Those unable to provide consent * Prisoners * Individuals unable to speak English

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