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The Preeclampsia Registry

Launched by PREECLAMPSIA FOUNDATION · Dec 18, 2013

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Preeclampsia Eclampsia Hellp Hellp Syndrome Toxemia Hypertensive Disorder Of Pregnancy Registry Pregnancy Complication Pregnancy Maternal Death Premature High Blood Pressure Hypertension

ClinConnect Summary

The Preeclampsia Registry is a clinical study aiming to gather important information about preeclampsia and related high blood pressure disorders that can occur during pregnancy, such as eclampsia and HELLP syndrome. By collecting data from women diagnosed with these conditions, their family members, and women who have never experienced preeclampsia, researchers hope to better understand why these disorders happen, how to predict them, and to explore new treatment options.

To participate in the study, women who have been diagnosed with preeclampsia or related conditions are eligible, as well as their female or male relatives. Women who have never had preeclampsia but wish to contribute as control participants are also welcome. Participants will be asked to provide information through questionnaires, and if a woman has passed away or is unable to participate due to a disability, a family member can step in to help. This study is currently recruiting individuals and is open to people of all ages, but those who can't provide consent, are prisoners, or do not speak English cannot participate. Your involvement could play a crucial role in advancing research on preeclampsia and improving outcomes for future mothers.

Gender

All

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

About Preeclampsia Foundation

The Preeclampsia Foundation is a leading nonprofit organization dedicated to advancing research, education, and advocacy for preeclampsia and related hypertensive disorders of pregnancy. Committed to improving maternal and infant health outcomes, the foundation collaborates with healthcare professionals, researchers, and affected families to promote awareness and foster innovative solutions. By sponsoring clinical trials and supporting scientific inquiry, the Preeclampsia Foundation aims to enhance understanding of these conditions, ultimately striving to reduce their incidence and improve care for those affected. Through its efforts, the foundation plays a critical role in transforming the landscape of maternal health.

Locations

Melbourne, Florida, United States

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Will be assessed yearly, up to 20 years

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