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NCT06573203

Clinical Effectiveness of Non-contact Heart Rate and Respiratory Rate Monitoring System

Active, enrolled NA Last updated 5 March 2025
What this trial tests

NA trial testing Non-contact heart rate and respiratory rate monitoring system in Sleep in 70 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
21 August 2024
Primary endpoint
31 August 2026
31 December 2026

Quick facts

Lead sponsorThe Children's Hospital of Zhejiang University School of Medicine
PhaseNA
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposediagnostic
Enrollment70
Start date21 August 2024
Primary completion31 August 2026
Estimated completion31 December 2026
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

The Children's Hospital of Zhejiang University School of Medicine

Who can join

Adults 1 Day to 1 Month, any sex, with Sleep or Infant,newborn. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

In this study, hospitalized neonates were taken as the focus of the study. The non-contact heart rate and respiratory rate monitoring system was used to measure heart rate, respiratory rate, sleep parameters, ECG monitor, neonatal sleep-wake scale, amplitude-integrated electroencephalography. aEEG), in order to provide a theoretical basis for standardizing the operation of medical staff and formulating sleep protection strategies in the future, so as to promote the sleep quality of hospitalized neonates and improve the prognosis of neonates.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Sleep

Currently open trials in the same condition.

Other The Children's Hospital of Zhejiang University School of Medicine trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06573203.

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