Nellcor™ Investigational Device Sitting-Walking Study

Medtronic

Status: Not yet enrolling

Conditions: Oxygen Saturation

Study type: Observational

Funder types: Industry

Identifiers

NCT07234279

MDT25003NPDSWF

Details and patient eligibility

About

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

Enrollment: 30 estimated patients

Sex: All

Ages: 18 to 75 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• 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

Participants must be a non-smoker or not have smoked within 36 hours prior to the study

Exclusion criteria

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

Morbid obesity (defined as BMI > 39.5)

Weight > 136 kg

Participants who self-report problems of unsteadiness or imbalance issues and/or who are unable to walk on a treadmill without holding onto the handrails

Participant self-reported known heart or cardiovascular conditions such as:

Uncontrolled hypertension (Systolic pressure ≥ 140mmHg or Diastolic pressure > 90mmHg on 3 consecutive readings day of screening)

Heart arrhythmias other than sinus arrhythmia (Self-reported and/or as identified on ECG day of screening).

History of heart attack, blocked artery, history of myocardial ischemia, angina, myocardial infarction, congestive heart failure, cardiomyopathy, stroke, transient ischemic attack, or carotid artery disease

Participants with self-reported clotting disorders, such as:

History of bleeding disorders or personal history of prolonged bleeding from injury

History of blood clots

Hemophilia

Current use of prescription blood thinner

Participants with other self-reported, known health conditions, such as:

Diabetes

Thyroid disease

Kidney disease / chronic renal impairment

History of seizures (except childhood febrile seizures), epilepsy, or unexplained syncope

Recent history of frequent migraine headaches, as determined medically relevant by the PI

History of head injury, as determined medically relevant by the PI

Cancer / chemotherapy

Sickle cell disease

History of hospital admission or a surgical procedure in the 60 days prior to study enrollment (self-reported)

Participants with any contraindications to protocol specific repositioning techniques

Unwillingness or inability to remove colored nail polish from test digit(s)

Participants who have self-reported health conditions beyond what is captured in the prior exclusion criteria, which in the opinion of the Investigator and/or Clinical Staff would classify the participant as medically unsuitable

Trial design

30 participants in 1 patient group

Healthy Volunteers

Description:

All subjects who meet the inclusion criteria and none of the exclusion criteria will be enrolled into the test group and will participate in data collection with use of the Nellcor™ Investigational device.