At a glance
ClinicalIndex Comparison RecordN/ACompleted· 20 enrolled
Drug / intervention
Nellcor USB Pulse Oximeter Monitor Interface Cabledevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Sensor Off Study Using a Nellcor USB Pulse Oximetry Monitor Interface Cable
In Brief
A clinical study evaluating Nellcor USB Pulse Oximeter Monitor Interface Cable for Healthy Volunteers. Completed, enrolled 20 participants across 1 site.
Detailed Summary
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.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHealthy Volunteers
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
201520162017201820192020202120222023202420252026
Enrollment StartSep 2014
First PostedOct 2014
Primary CompletionNov 2014
TodayJul 2026
First PostedOct 16, 2014
Enrollment StartSep 1, 2014
Primary CompletionNov 1, 2014
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 11.7 years ago
Interventions
Nellcor USB Pulse Oximeter Monitor Interface Cabledevice
Volunteers are subjected to certain simulated, sensor removal conditions known to represent challenges to the sensor-off feature. Such conditions include exposing the sensor to an ambient light source, sensor slipping off the finger with the light emitter and detector facing each other or a sensor slipping off under a blanket.