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Klinische Studie

Pediatric/Adolescent WatchPAT 400 Reliability Pilot Study

NCT: NCT07851402 · NOT_YET_RECRUITING

NCT-IDNCT07851402
Medizinische Daten: StatusNOT_YET_RECRUITING
Startdatum2026-12-01
Abschluss2028-12-01
SponsorMilton S. Hershey Medical Center (OTHER)
First posted
Last updated

Kurzzusammenfassung

The goal of this clinical trial is to learn whether a newer sleep-testing device gives results that closely match the standard overnight sleep study, in children and adolescents ages 6-18 who are being evaluated for possible sleep apnea. The main questions it aims to answer are: Does the new device (WatchPAT 400) give breathing and oxygen level results that agree with the standard overnight sleep study (polysomnography)? How reliably can two doctors, each looking at only one test's results, arrive at similar conclusions about a child's sleep apnea? Participants will: Have their regular, already-scheduled overnight sleep study performed exactly as usual Wear the WatchPAT 400 device (a small sensor on one finger, a wrist unit, and one adhesive patch on the chest) at the same time, during that same night Have both sets of results reviewed separately by two different study doctors Researchers will compare the results from the WatchPAT 400 device to the results from the standard sleep study to see how closely they agree, and how well the new device performs at detecting sleep apnea in children and teenagers.

Offizielle Quelle

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