Sensor Off Study Using a Nellcor USB Pulse Oximetry Monitor Interface Cable

Medtronic

Status: Completed

Conditions: Healthy Volunteers

Treatments: Device: Nellcor USB Pulse Oximeter Monitor Interface Cable

Study type: Interventional

Funder types: Industry

Identifiers

NCT02265783

COVMOPR0461

Details and patient eligibility

About

The purpose of this study is to validate that the device posts a Sensor-Off message within the time frame stated in the proposed claims.

Enrollment: 20 patients

Sex: All

Ages: 18 to 50 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Male or female subjects 18 or older (inclusive)
• Subject is able to participate for the duration of the study
• Subject is willing to sign an informed consent

Exclusion criteria

• Previous injury or trauma to fingers or hands that may change blood flow or vascular supply and affect our 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

Trial design

Primary purpose: Device Feasibility

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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20 participants in 1 patient group

Nellcor USB Pulse Oximeter Monitor Interface Cable Sensor Test

Other group

Treatment:

Device: Nellcor USB Pulse Oximeter Monitor Interface Cable