Comparison of Perfusion Index Monitoring Using a Smartwatch and a Pulse Oximeter

ConditionPerfusion Index

Trial statusNot yet recruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

Age18+

SponsorCzech Technical University in Prague

About this trial

The aim of the study is to experimentally compare measured perfusion index values between smartwatch and a medical grade pulse oximeter in healthy subjects at rest and with and without motion artifacts and during exercise.

Eligibility criteria

Qualifiers

Healthy Adult Volunteer

Disqualifiers

Post-traumatic upper limb conditions affecting finger or arm perfusion

Injuries or diseases of the skin of the fingers and arm

Any acute phase of any disease

Trial design

Treatments tested in this trial

Resting conditions
Movement artifacts
Circulation constriction
Physical exercise

Treatment groups

50 Participants

are divided into 1 treatment group

Locations

This trial has no locations

Sponsors and collaborators

Czech Technical University in Prague

Lead sponsor

Source ClinicalTrials.gov