Evaluation of an Investigational Wearable Vital Signs Monitoring Device in Healthy Infants

Description

The primary objective of this study is to evaluate the feasibility of the use of an investigational wearable vital sign monitoring device in infants.

Conditions

Congenital Heart Disease in Children

Study Overview

Study Details

Study overview

The primary objective of this study is to evaluate the feasibility of the use of an investigational wearable vital sign monitoring device in infants.

Evaluation of an Investigational Wearable Vital Signs Monitoring Device in Healthy Infants

Evaluation of an Investigational Wearable Vital Signs Monitoring Device in Healthy Infants

Condition
Congenital Heart Disease in Children
Intervention / Treatment

-

Contacts and Locations

Baltimore

Johns Hopkins Children's Center, Baltimore, Maryland, United States, 21287

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Patient admitted to either the newborn nursery, pediatric cardiac intensive care unit (PCICU), or pediatric care unit (PCU)
  • * Parent provided written informed consent
  • * Foster or ward of the state

Ages Eligible for Study

1 Day to 1 Year

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Johns Hopkins University,

Danielle Gottlieb Sen, MD, PRINCIPAL_INVESTIGATOR, Johns Hopkins School of Medicine

Study Record Dates

2025-12-31