At a glance
ClinicalIndex Comparison RecordN/ACompleted· 28 enrolled
Drug / intervention
INVSENSOR00013device
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.
INVSENSOR00013 Respiratory Rate Clinical Performance Study
In Brief
A clinical study evaluating INVSENSOR00013 for Healthy. Completed, enrolled 28 participants across 1 site.
Detailed Summary
The objective of this prospective study is to compare the noninvasive respiration from pleth (RRp) performance of the Masimo INVSENSOR00013 device against the respiratory rate measured by capnography (RRref), Masimo's RAM technology and the manual annotation.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHealthy
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
201820192020202120222023202420252026
Enrollment StartFeb 2018
Primary CompletionFeb 2018
First PostedFeb 2018
TodayJul 2026
First PostedFeb 22, 2018
Enrollment StartFeb 6, 2018
Primary CompletionFeb 14, 2018
TodayJul 2, 2026
Enrollment to primary: 8 daysPosted 8.4 years ago
Interventions
INVSENSOR00013device
Investigational pulse oximeter device that will be placed on the subject's finger. This will be used as a spotcheck device