AzTrials
AzTrials

Congenital Heart DiseaseNCT06818760

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

An observational study of Congenital Heart Disease and Congenital Vascular Disorder, run by The Cleveland Clinic at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial summary

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. Read more about this study

Who is it for?
Ages 18 years and older, women only
What is being tested?
Masimo Smart Wristband
How many people
50 participants
Where
1 siteUnited States
Study dates
27 Jan 2025to 31 Dec 2028
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Women only
  • No healthy volunteers
  • Adult, Older adult

Study population: Women greater or equal to 18 years of age who have a congenital heart disease (congenital valvular heart disease, Native valvular heart disease, bioprosthetic valvular heart disease, any mechanical valve prosthesis and congenital cardiomyopathy with EF less then 50%) who are pregnant from high risk obstetric clinic.

Who may be able to join

  • Women evaluated in the cardio-obstetrics clinic either prepartum, intrapartum, or postpartum with congenital heart disease.
  • Congenital heart disease: Based on modified World Health Organization (mWHO) classification of maternal cardiovascular disease group ≥ II.
  • mWHO Class I include mild pulmonary stenosis, uncomplicated patent ductus arteriosus, and repaired shunts, to be excluded.
  • mWHO Class II includes unoperated atrial septal defect or ventricular septal defect and repaired tetralogy of Fallot.
  • mWHO Class II-III includes mild left ventricular impairment, valvular heart disease not in class I, repaired aortic coarctation, Marfan without aortic dilation, bicuspid aortic valve with <45 mm root, hypertrophic cardiomyopathy.
  • mWHO Class III includes systemic right ventricle, Fontan circulation, unrepaired cyanotic heart disease, Marfan with aorta 40-45 mm, bicuspid aortic valve with root 45-50 mm, other complex congenital heart disease (such as Shone complex).
Show all 16Show fewer
  • mWHO Class IV includes Marfan with >45 mm aorta, bicuspid aortic valve with > 50 mm aorta, severe systemic ventricular dysfunction (EF<30%), severe symptomatic AS or MS, native severe coarctation, all severe pulmonary hypertension patients from any cause.
  • Congenital valvular heart disease:
  • Native valvular heart disease: tricuspid, pulmonary, mitral and aortic with ≥ moderate regurgitation or stenosis by echocardiography.
  • Bioprosthetic valvular heart disease with ≥ moderate regurgitation or stenosis by echocardiography.
  • Any mechanical valve prosthesis
  • Congenital Cardiomyopathy
  • Cardiomyopathy with EF < 30%
  • Cardiomyopathy with EF 30-50%
  • Provide Informed consent
  • Age > 18 years of age

Who cannot join

  • Patients on hemodialysis

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Joanna Ghobrial, MD contact

216-444-5923

GHOBRIJ@ccf.org

United States1 site, 1 recruiting
  • Cleveland Clinic

    Cleveland, Ohio, 44195

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

    Justin Lappen, MD

    Recruiting

Other trials in United States

About this study

Official title: Single Center Pilot Study of Remote Monitoring in Pregnant Women With Congenital Heart Disease Using Wrist Wearables

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.

Read the detailed description

Maternal cardiovascular disease (MCD) remains the leading cause of death in pregnant women, especially in the United States, where heart disease is on the rise. The worse outcomes disproportionately affect disadvantaged populations, including those with poor access to healthcare, and ethnic minorities. Reducing maternal mortality is a World Health Organization global health goal, and multiple efforts have been initiated to both study maternal cardiac disease as well as reduce morbidity and mortality. At least half of serious cardiac complications can be prevented with closer monitoring and adequate care. A multidisciplinary approach using the Cardio-obstetrics clinic model has been shown to improve outcomes in women with cardiovascular disease, but successful efforts have been limited to comprehensive care centers in larger cities. Over the past decades, there have also been advances in the risk assessment for pregnant women with cardiac disease, but all risk models have not been as accurate in validation models and further research is warranted.

Hemodynamic changes of pregnancy, during labor, and in the early postpartum period include a decrease in systemic vascular resistance (SVR) and increases in blood volume and heart rate, all resulting in increased cardiac output (CO). There is also an associated increase in ventricular muscle mass and end diastolic volumes with improved systolic function, but without a pathologic increase in end-diastolic pressures. Such hemodynamic and anatomic alterations can exacerbate underlying cardiac disease, as well as uncover previously unrecognized cardiovascular pathology, thereby increasing the risk of cardiac complications.12 Several cardiac complications during pregnancy and in the postpartum period are due to the inapt response to pregnancy with either an inability to augment CO or inability to tolerate the increased CO. Addressing maternal cardiac complications would require earlier detection and identification of those at risk.

Wearable derived biomarkers: Physiological health parameters derived from either non-invasive monitors or wearables allow continuous tracking of such parameters in an ambulatory state:

  • Pulse Oximetry (SpO2) is used to detect peripheral cyanosis, normal being >95%, and has been used to detect newborn cyanosis in children with congenital heart disease, albeit with reduced accuracy at saturations <60%.
  • Respiratory rate in breaths per minute (RRp) can increase in pregnancy from 8-12 breaths per minute to 15-17 breaths per minute, but it increases to a larger extent in states of distress, infection, and cardiovascular decompensation. In one study, increased RRp, and heart rate (HR) were detected early in women that were found to have an intraamniotic infection, demonstrating the benefit of such monitors in early detection of pathology.
  • Heart rate variability (HRV) measures changes in the time intervals between consecutive heartbeats and is a surrogate for neural cardiac control and the balance between the sympathetic and parasympathetic drive. Higher variability (50-100 ms) is normal with an overall decline with age. Low HRV has been shown to be a predictor of poor outcomes in patients with cardiac disease in small studies, a wearable device was used to evaluate HRV during normal pregnancy, and it was found to be overall decreased (50-70 ms), but with a dynamic burst in autonomic activity in the transition from second to third trimester
  • In addition, these monitors can provide dynamic indices that include the perfusion index (Pi), which depends on the blood flow in the peripheral circulation, the cardiac output, and the vascular tone, which is calculated from the amount of light constantly absorbed by skin from non-pulsatile blood, and the variable amount of light absorbed by pulsating arterial inflow, with values ranging from 0.2%-20%, with lower percentages indicating lower perfusion state. There have been unvalidated suggestions that Pi can be used as a surrogate for CO.
  • The pleth variability index (PVi), is the maximal and minimal Pi over a respiratory cycle and is also expressed in %, with a range of 9-13%. In a randomized controlled trial of intraoperative and postoperative patients, elevated PVi was used to direct fluid management by administering crystalloid infusions in PVi >13%, with appropriate fluid responsiveness. Such intervention reduced the overall fluid infused to patients, and reduced lactate levels. Elevated PVi has also been used to predict hypotension in pregnant women undergoing c-section.

Masimo® noninvasive monitors (Masimo Corp, Irvine, CA) are FDA approved for use in adults and newborns to provide real time pulse oximetry (SpO2) and heart rate. Masimo has CE mark for additional parameters which include PVR, atrial fibrillation respiratory rate per minute (RRp), heart rate variability (HRV), and PVi. Clinical studies demonstrated they are motion-tolerant, report functional oxygen saturation, and validation in low perfusion conditions. Smart wristbands are an unobtrusive, and promising novel method to monitor ambulatory health parameters throughout pregnancy. The Masimo W1® wristband is FDA approved and uses clinically tested technology in a wearable patient-friendly format. Compliance with wearable devices has been demonstrated in a small study of 20 pregnant women where it was worn approximately 6 out of 7 months, with a slight drop in adherence postpartum.

Being tested
Masimo Smart Wristband
Medical subject headings
Heart Defects, Congenital, Cardiomyopathy, infantile histiocytoid

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Masimo Smart WristbandDiagnostic test

    Continuous wear of Masimo Smart Wristband

Study groups in NCT06818760
Study groupRoleWhat they receive
Masimo Smart WristbandMasimo Smart Wristband continuous ambulatory monitoring
Receives: Diagnostic Test: Masimo Smart Wristband

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. New onset atrial or ventricular arrhythmias

    New onset of atrial tachycardia, flutter or fibrillation, non-sustained VT (3 or more PVC, lasting <30 seconds), PVC burden >10% within 24 hours detected on ECG or event monitors on clinic visits or prompted by subjective palpitations, ECG or event monitor obtained routinely due to clinical suspicion of arrhythmia.

    Measured: Up to 12 month post-partum

Secondary outcomes (5)
  1. Increased NT-proBNP

    Change in value of >200 pg/mL in the first and second trimester, and >150 pg/mL in the third trimester

    Measured: During the first (up to 12 weeks of gestation) and third trimester (28-40 weeks of gestation)

  2. New or worsening of biventricular dysfunction or valvular dysfunction on echocardiography

    a reduction in EF by >5%. New or worsening valvular dysfunction is defined as an increase in valve dysfunction by 1 grade of severity (mild, moderate, severe) on echocardiography.

    Measured: Up to 12 months post-partum

  3. Cardiac-related hospital or intensive care unit (ICU) admission

    Number of occurrence of cardiac-related hospital or ICU admission

    Measured: Up to 12 months post-partum

  4. Inotropic or mechanical circulatory support

    Number of occurrence of inotropic or mechanical circulatory support

    Measured: Up to 12 months post-partum

  5. Cardiac death

    Occurrence of death from cardiac-cause

    Measured: Up to 12 months post-partum

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted10 Feb 2025
  2. Study start27 Jan 2025
  3. Primary completion31 Dec 2028 (estimated)
  4. Study completion31 Dec 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
50 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06818760
Sponsor's protocol ID
24-1183
Status last verified
Feb 2026
First submitted
5 Feb 2025
Last updated
13 Feb 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Congenital Heart Disease and Congenital Vascular Disorder, run by The Cleveland Clinic at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 16 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 13 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Joanna Ghobrial, MD (216-444-5923, GHOBRIJ@ccf.org), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

New onset atrial or ventricular arrhythmias (time frame: Up to 12 month post-partum). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Feb 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in