Nellcor™ Investigational Device Sitting-Walking Study
ConditionOxygen Saturation
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-75
SponsorMedtronic - MITG
About this trial
To examine pulse rate and blood oxygen saturation accuracy of the Nellcor™ Investigational Device during non-motion and walking motion conditions in a diverse patient population through non-invasive means
Eligibility criteria
Qualifiers
Male or female participants ≥18 years of age, and <75 years of age.
Participant is able to participate for the duration of the study
Participant is willing to sign an informed consent form (ICF)
Participant weighs > 40kg
Disqualifiers
Participant self-reported prior injury or trauma to fingers or hands, which in the opinion of the investigator, may change blood flow or vascular supply and affect the ability to test sensors
Physiologic abnormalities that prevent proper application of pulse oximetry sensor
Severe contact allergies that cause a reaction to standard adhesive materials such as those found in medical sensors and electrodes
Individuals of childbearing potential who are self-reported as pregnant, or who are self-reported as trying to get pregnant
Trial design
Treatments tested in this trial
- Not listed
Trial groups
30 Participants
are grouped into 1 trial groupLocations
Sponsors and collaborators
Source ClinicalTrials.gov