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Clinical Trials/NCT06439511
NCT06439511
Completed
Not Applicable

Comparison of a Non Contact Vital Signs Application (Darwin Edge rVSM) on a Smartphone With Traditional Pulse Oximetry for Heart Rate Measurement: a Prospective Clinical Study

Hôpital du Valais1 site in 1 country200 target enrollmentJuly 1, 2024
ConditionsHeart

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Heart
Sponsor
Hôpital du Valais
Enrollment
200
Locations
1
Primary Endpoint
Heart rate
Status
Completed
Last Updated
last year

Overview

Brief Summary

The investigators want to test the accuracy of the Smartphone application Darwin Edge rVSM in measuring heart rate, as compared to traditional pulsoxymetry. The intervention is to look at the smartphone camera for approximately 30 seconds, and after that to compare the heart rate value with that obtained with a recording by pulsoxymetry.

Detailed Description

Participants undergoing a routine perianesthetic consultation at the preanesthetic clinic will be recruited. as a part of routine clinical assessment their heart rate is measured with pulsoxymetry, a non invasive device worn at the fingertip for about 1 minute. this measurement will be compared to the values for heart rate that can be obtaine with the ''Darwin Edge rVSM'' mobile application. this application can be installed on any smartphone. the participant is required to look into the smartphone camera for about 30 seconds. environmental and lighning conditions will be kept stable. The investigators will do the measurements in 200 participants in order to obtaine values in a population characterized by a variety of phenotypes, in the perioperative setting.

Registry
clinicaltrials.gov
Start Date
July 1, 2024
End Date
October 31, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Men or women older than 18 years old presenting to the preanesthetic assessment clinic of Valais Hospital
  • Subjects that have signed the informed consent form
  • Exclusion criteria:
  • subjects with damaged/injured skin at the face
  • Subjects unable to remain still for 30 seconds

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Heart rate

Time Frame: 1 minute

accuracy of heart rate measurement

Study Sites (1)

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