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

• Conditions: Indication for Modification of Patient's Cardiopulmonary Status

• Registration Number: NCT01592877
• Lead Sponsor: Holux Technology, Inc.

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.

Study Timeline

• Study Start: 2011-12
• Study First Submitted: 2012-05-04
• Study First Submitted QC: 2012-05-04
• Study First Posted: 2012-05-07
• Status Verified: 2012-07
• Last Update Submitted: 2012-07-30
• Last Update Posted: 2012-07-31
• Primary Completion: 2012-10
• Study Completion: 2012-10

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

• conscious adult,
• > 18 years old

Exclusion Criteria

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

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Trial Locations

Locations (1)

Shin Kong Wu Ho-Su Memorial Hospital; 🇨🇳 Taipei, Taiwan