New registry aims to uncover hidden risks for pregnant women with heart disease
NCT ID NCT04828070
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This registry follows 75 pregnant women with heart disease to better understand the risks and outcomes for both mother and baby. Researchers will track health data for one year and check vital status at five years. The goal is to fill knowledge gaps and improve future care for this group.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this registry could provide crucial data to guide better care and reduce risks for pregnant women with heart disease.
- What could go wrong
- This is an observational registry, not a treatment trial. It will not directly improve outcomes and may face challenges in collecting complete data.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 75 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2020
- Expected to finish
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Jun 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Pregnant women with cardiovascular disease
- Ages
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18 to 55 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Aged 18 and older * Pregnant at any point in gestation (with singleton or multiple gestation) * History of congenital and/or acquired heart disease defined as the following: * valvular, congenital, ischemic heart disease or cardiomyopathy, * clinically significant maternal arrhythmias in women, * current or previous history of peripartum cardiomyopathy, * supraventricular tachycardia, * placement of either a pacemaker or electrical assist device, * aortopathies (Marfan syndrome, Loey's Deitz, Ehlers Danlos \[vascular subtype\], * pre-pregnancy diagnosis of pulmonary hypertension * English- or Spanish-speaking Exclusion Criteria: * Unable to provide written informed consent
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Saint Luke's Hospital of Kansas City
Kansas City, Missouri, 64111, United States
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