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Study identifier: NCT06818760 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Remote Monitoring in Pregnant Women With Congenital Heart Disease Using Wrist Wearables

Condition: Congenital Heart Disease · Congenital Vascular Disorder · Congenital Cardiomyopathy  ·  Sponsor: The Cleveland Clinic

PhaseN/A
Planned participants50
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

Congenital heart disease (CHD) includes a wide variety of types of disease, including congenital abnormalities of the heart valves. This can range from bicuspid aortic valve and other aortic valve deformities to more complex disease such as tetralogy of Fallot. For many kinds of CHD, the optimal timing of interventions remains unclear. For instance, in tetralogy of Fallot, there is still equipoise about when to offer pulmonary valve replacement (PVR), while in aortic regurgitation, some patients can remain stable for many years. The primary focus of this study is to use continuous physiologic data (CPD), obtained using wearable biosensors (a type of biometric monitoring technology), to develop improved biomarkers of disease progression and prognosis from patients with congenital heart disease (CHD) who are pregnant while they are at home as well as looking at patients' experience and interaction with wearable biosensor technology at home.

This description comes directly from the study's public registry record.

Talk to the study team

Joanna Ghobrial, MD  ·  216-444-5923  ·  GHOBRIJ@ccf.org

Always discuss trial participation with your own doctor first.

Locations (1)

Cleveland ClinicCleveland, Ohio, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06818760