Accuracy Validation of a Pulse Oximetry Monitor

Healthy Clinical Trial

Official title:

SpO2 Accuracy Validation of a USB Pulse Oximetry Monitor Interface Cable Via Reference Co-Oximetry

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT02506010
• Other study ID #: COVMOPR0499
• Status: Withdrawn
• Phase: N/A
• First received: July 14, 2015
• Last updated: October 14, 2016
• Start date: November 2016
• Est. completion date: January 2017

Study information

• Verified date: October 2016
• Source: Medtronic - MITG
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Observational

Clinical Trial Summary

The purpose of this study is to conduct an oxygen saturation (SpO2) accuracy validation comparing prototype pulse oximeter oxygen saturation measurements directly to arterial blood saturation during non-motion conditions over the range of 60-100% SaO2 as measured by Reference CO-Oximetry. Additionally, the prototype pulse oximeter pulse rate measurements will be compared to 3-lead ECG heart rate measurements made via a multi-parameter monitor.

Description:

The description of this study is to conduct an oxygen saturation (SpO2) accuracy validation comparing prototype pulse oximeter oxygen saturation measurements directly to arterial blood saturation during non-motion conditions over the range of 60-100% SaO2 as measured by Reference CO-Oximetry. Additionally, the prototype pulse oximeter pulse rate measurements will be compared to 3-lead ECG heart rate measurements made via a multi-parameter monitor.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: January 2017
• Est. primary completion date: January 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 45 Years

Eligibility

Inclusion Criteria:

• healthy

• non-smoking, or who have refrained from smoking for 2 days

• male or female of any race

• 18-45 years.

• Subjects must have the ability to understand and provide written informed consent as well as be willing to comply with study procedures.

• To be eligible to participate in the study, the subject must clear a recent physical (12-lead ECG, medical history and blood test for sickle cell disease.) prior to enrollment

Exclusion Criteria:

• - morbid obesity (defined as BMI > 39.5),

• injuries, deformities or abnormalities or piercings that may prevent proper application of the device under test, compromised circulation,

• subjects with known respiratory conditions (smokers with COHb levels >3%, flu, pneumonia, bronchitis, shortness of breath/ respiratory distress, severe asthma, emphysema, COPD),

• subjects with known heart or cardiovascular conditions (uncontrolled hypertension, heart arrhythmias other than sinus arrhythmia, previous heart attack, blocked artery, history of myocardial ischemia, angina, myocardial infarction, congestive heart failure or cardiomyopathy, history of stroke, transient ischemic attack or carotid artery disease),

• other known health condition (diabetes, thyroid disease, kidney disease / chronic renal impairment, history of seizures (except childhood febrile seizures) or epilepsy, or unexplained syncope, recent history of frequent migraine headaches, recent head injury, cancer / chemotherapy

• women actively trying to get pregnant or are pregnant,

• clotting disorders (history of bleeding disorders or current use of blood thinners, Hemophilia, blood clots)

• Sickle cell disease

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

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

• Prior or known allergies to: lidocaine (or similar pharmacological agents, e.g., Novocain) or heparin

• Recent arterial cannulation (i.e., less than 30 days prior to study date), Six or more arterial cannulations of each (right & left) radial artery, history of clinically significant complications from previous arterial cannulation

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

• Healthy

Locations

Country	Name	City	State
United States	Clinimark	Louisville	Colorado

Sponsors (2)

Lead Sponsor	Collaborator
Medtronic - MITG	Clinimark, LLC

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The OxiCable pulse rate measurement performance is an ARMS of 3 or better over the full range 60-100% SaO2.		2.5 hours	No