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Advancing the Science of Pediatric Interstage Home Monitoring

NCT06547268 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 2

Last updated 2025-10-31

No results posted yet for this study

Summary

The overall goal of this study is to understand the feasibility of using a wireless sensor device (instead of a wired device) to collect information used to monitor children with heart conditions at home.

Conditions

  • Heart Defects, Congenital

Interventions

DEVICE

Wireless sensor and platform

Skin-mounted sensor that pairs with tablet platform

Sponsors & Collaborators

  • Sibel Health Inc.

    collaborator INDUSTRY

  • Ann & Robert H Lurie Children's Hospital of Chicago

    lead OTHER

Principal Investigators

  • Carolyn C Foster, MD, MS · Ann and Robert H. Lurie Children's Hospital of Chicago

Eligibility

Max Age
2 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-07-24
Primary Completion
2025-10-30
Completion
2025-10-30
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06547268 on ClinicalTrials.gov