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A Comparative Study of the Performance of a New Type Non-contact Patient Monitor

Clinical Test of Ultra-Wideband Non-contact Heart Rate and Breath Rate Monitor

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01592877
Enrollment
50
Registered
2012-05-07
Start date
2011-12-31
Completion date
2012-10-31
Last updated
2012-07-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Indication for Modification of Patient's Cardiopulmonary Status

Keywords

UWB, non-contact, patient monitor

Brief summary

To verify the accuracy and reliability of the ultra wideband (UWB) non-contact breath rate and heart rate monitor, ICU bedside monitor is used as the gold standard.

Detailed description

In this study, 50 volunteer patients are tested on the UWB non-contact breath rate and heart rate monitor. The testing time length for each patient is set to two hours. Subject is not to be restrained and nurse is allowed to take care the subject while testing. The breath rate and heart rate data will be analyzed for their accuracy against the MP60 (Philips) bedside monitor.

Interventions

None listed

Sponsors

Shin Kong Wu Ho-Su Memorial Hospital
CollaboratorOTHER
Holux Technology, Inc.
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* conscious adult, * \> 18 years old

Exclusion criteria

* non-conscious, * pregnant women, * epilepsy patients, * patients with heart pacemaker or ACIDS, * patients on respirator

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026