SpO2 Accuracy Low Saturation Validation of the OxySoftN Sensor

Hypoxia Clinical Trial

Official title:

SpO2 Accuracy Validation of the OxySoftN Sensor Via Reference CO-Oximetry in Healthy, Well-Perfused Subjects

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04811963
• Other study ID #: MDT20028OXYLOV
• Status: Completed
• Start date: April 6, 2021
• Est. completion date: April 9, 2021

Study information

• Verified date: May 2021
• Source: Medtronic - MITG
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

To compare prototype pulse oximeter saturation measurements, during normal to low saturation, to saturation measurements made by a multi-wavelength CO-oximeter, taken from arterial blood samples from healthy human subjects.

Description:

The study utilizes a single-site, physiology laboratory (Clinimark) for non-randomized, prospective, observational studies. The goal is to enroll a minimum of ten subjects. Subjects may be of any race, ranging in pigmentation from light to dark to meet the study design requirements.

The general purpose of Invasive Controlled Desaturation Studies is to validate the SpO2 and pulse rate accuracy in comparison to reference-standard measurements of blood SaO2 by a CO-oximeter during low saturation conditions. This is achieved through paired observations of SpO2 and SaO2 values over the specified SpO2 accuracy range of 60 % to 100 % SaO22 of the prototype pulse oximeter on a group of healthy adult volunteers. The fraction of inspired oxygen (FiO2) delivered to test subjects is varied to achieve a series of targeted steady-state saturation periods. Arterial blood samples are periodically taken from an indwelling arterial catheter for use in the comparison.

Pulse rate accuracy will be evaluated during the same data collection period as SpO2. Pulse rate will be compared to reference ECG heart rate. In the unlikely event that the ECG monitor malfunctions, the Pulse rate reference may be taken using the average pulse rate value from the transfer standard pulse oximeters. This study is designed to support an FDA submission for pulse rate and saturation accuracy in a diverse subject population during low saturation conditions over a specified saturation range for the OxySoftN pulse oximetry system.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 10
• Est. completion date: April 9, 2021
• Est. primary completion date: April 9, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

1. Subject must have the ability to understand and provide written informed consent

2. Adult subjects 18 to 50 years of age.

3. Subject must be willing and able to comply with study procedures and duration.

4. Subject is a non-smoker or who has not smoked within 2 days prior to the study.

5. Male or female of any race.

6. Cleared same day Health Assessment form and health screening.

7. Cleared physical exam by a licensed physician, physician assistant, or advanced practice nurse (medical exam includes 12-lead ECG, medical history and blood test to show no sickle cell disease present)

8. Successful Perfusion Index Ulnar/Ulnar+Radial Ratio test showing adequate collateral blood flow.

Exclusion Criteria

1. Subject is considered as being morbidly obese (defined as BMI >39.5)

2. Compromised circulation, injury, or physical malformation of fingers, hands, ears or forehead/skull or other sensor sites which would limit the ability to test sites needed for the study. (Note: Certain malformations may still allow subjects to participate if the condition is noted and would not affect the sites utilized.)

3. Females of childbearing potential, who are pregnant, who are trying to get pregnant or who have a urine test positive for pregnancy on the day of the study

4. Subjects with COHb levels >3% as assessed by CO-Oximetry during the procedure

5. tHb < 10 g/dl as assessed by CO-Oximetry during the procedure

6. MetHb = 2% as assessed by CO-Oximetry during the procedure

7. Subjects with known respiratory conditions such as:

1. uncontrolled / severe asthma,

2. flu or influenza type infection

3. pneumonia / bronchitis,

4. shortness of breath / respiratory distress,

5. unresolved respiratory or lung surgery,

6. emphysema, COPD, lung disease

8. Subjects with known heart or cardiovascular conditions such as:

1. Hypertension: systolic >140mmHg, or Diastolic >90mmHg on 3 consecutive readings.

2. have had cardiovascular surgery

3. Chest pain (angina)

4. heart rhythms other than a normal sinus rhythm or

5. with respiratory sinus arrhythmia

6. previous heart attack

7. blocked artery

8. unexplained shortness of breath

9. congestive heart failure (CHF)

10. history of stroke

11. transient ischemic attack

12. carotid artery disease

13. myocardial ischemia

14. myocardial infarction

15. cardiomyopathy

9. Self-reported health conditions as identified in the Health Assessment Form

1. diabetes,

2. uncontrolled thyroid disease,

3. kidney disease / chronic renal impairment,

4. history of seizures (except childhood febrile seizures),

5. epilepsy,

6. history of unexplained syncope,

7. recent history of frequent migraine headaches,

8. recent symptomatic head injury, within the last 2 months

9. Subjects with known clotting disorders

10. history of bleeding disorders or personal history of prolonged bleeding from injury

11. history of blood clots

12. hemophilia

13. current use of blood thinner: prescription or daily use of aspirin

14. Subjects with Severe contact allergies to standard adhesives, latex or other materials found in pulse oximetry sensors, ECG electrodes, respiration monitor electrodes or other medical sensors

15. Subjects with prior or known severe allergies to lidocaine (or similar pharmacological agents, e.g. Novocain) or heparin

16. Arterial cannulation within the last 30 days prior to study date, (this may exclude only one radial artery site. Left or right)

17. History of clinically significant complications from previous arterial cannulation.

18. A radial artery with ten or more arterial cannulations right or left, excludes that site.

19. Unwillingness or inability to remove colored nail polish or colored artificial nails other than clear from test digits.

20. Other known health condition, should be considered upon disclosure in Health Assessment form

Related Conditions & MeSH terms

• Desaturation of Blood
• Hypoxia

Intervention

Device:
• Non-Invasive Controlled Hypoxia
Following arterial cannulation, hypoxia is induced by reducing the percent of inspired oxygen the subject breathes while simultaneous measurements are recorded from the test pulse oximeters and arterial blood samples are collected at targeted levels of saturation.

Locations

Country	Name	City	State
United States	Clinimark	Louisville	Colorado

Sponsors (1)

Lead Sponsor	Collaborator
Medtronic - MITG

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To investigate performance of the OxySoft device by measuring oxygen saturation accuracy over a Low Saturation range of 60-80%	To validate the proposed claims for saturation accuracy in a diverse subject population during Low Saturation over a specified saturation range. The acceptance criteria for the OxySoftN Sensor SpO2 during Low Saturation conditions across the saturation range of 60-80% when paired with the N-600x, PM1000N and Oxicable: SpO2 OxySoftN ± 3% (Arms)	April 2021