Preeclampsia Clinical Trials

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PRoteomics and EchoCardiography for Identifying Subclinical Cardiac Dysfunction in Preeclampsia (PRECISE)

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

The goal of this study is to find and confirm blood-based markers (called proteins) that may show early heart changes in women with preeclampsia, even before symptoms appear. It will also use heart ultrasound (echocardiography) to look at patterns of how the heart changes during pregnancy in women with preeclampsia. The main questions it aims to answer are: * Do these blood markers relate to heart changes on ultrasound? * How may they help predict future health problems for the mother? Participants will: * Complete a 20-minute survey that will include taking your baseline demographic information, clinical information/medical history, asking about pre-existing health conditions, including measuring your height, weight, and blood pressure. * Have transthoracic echocardiography (TTE) performed at 12 - 16 weeks gestation and again at 28 - 32 weeks gestation. * Provide a blood sample for these protein measurements. These samples will be collected at intake (12 - 16 weeks gestation) and again at 28 - 32 weeks gestation.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 13
Maximum Age: 50
Healthy Volunteers: t
View:

• • Pregnant women who are up to 20 weeks pregnant

‣ Able to consent to participate in the study

⁃ Are enrolled in the ENHANCE-CVH study

⁃ Willing to undergo echocardiography and blood draws

Locations
Other Locations
Nigeria
University of Abuja Teaching Hospital
RECRUITING
Abuja
Contact Information
Primary
Zainab Mahmoud, MD, MSc
zmahmoud@wustl.edu
314-415-0009
Backup
Cecilia Nartey, MBChB, MPH
c.nartey@wustl.edu
314-528-1082
Time Frame
Start Date: 2026-04-24
Estimated Completion Date: 2027-12
Participants
Target number of participants: 172
Treatments
Single cohort
Single cohort of pregnant participants who are up to 20 weeks pregnant at enrollment
Related Therapeutic Areas
Sponsors
Leads: Washington University School of Medicine
Collaborators: Vanderbilt University Medical Center, University of Abuja Teaching Hospital

This content was sourced from clinicaltrials.gov