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Study identifier: NCT04626154 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Thoracoabdominal Asynchrony and Respiratory Distress

Condition: Respiratory Insufficiency  ·  Sponsor: Massachusetts General Hospital

PhaseNA
Planned participants20
Who can joinAll sexes, 28 Days to 17 Years
Healthy volunteersNo

About this study

The investigators hypothesize that a simple 3-point tracking device that uses motion sensors attached to the abdomen and chest of a child will provide information regarding thoracoabdominal asynchrony (TAA), a major component of respiratory distress, and ultimately help guide a clinician to initiate, escalate, de-escalate, or stop respiratory support interventions. AIMS To determine if the TAA-monitoring device can be used to detect differences in respiratory synchrony in a manner that is clinically applicable. The investigators hope that the device will detect 1) major asynchrony events in a timely manner so as to prompt clinician intervention during future use; and 2) asynchrony events that may be less visible to the naked eye that may be precursors to more severe events.

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

Talk to the study team

Ryan Carroll, MD, MPH  ·  7733328178  ·  rcarroll4@mgh.harvard.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Massachusetts General HospitalBoston, Massachusetts, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT04626154