At a glance
ClinicalIndex Comparison RecordN/ACompleted· 27 enrolled
Drug / intervention
INVSENSOR00032 and INVSENSOR00033device
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.
INVSENSOR00032 and INVSENSOR00033 Respiration Rate Clinical Performance Study
In Brief
A clinical study evaluating INVSENSOR00032 and INVSENSOR00033 for Healthy. Completed, enrolled 27 participants across 1 site.
Detailed Summary
This study compares the performance of respiration rate from pleth measured prospectively with either INVSENSOR00032 and/or INVSENSOR00033 devices against the respiration rate derived from the manual scoring of the capnography waveform in healthy adult subjects.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHealthy
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20192020202120222023202420252026
Enrollment StartFeb 2019
Primary CompletionFeb 2019
First PostedApr 2019
TodayJul 2026
First PostedApr 1, 2019
Enrollment StartFeb 13, 2019
Primary CompletionFeb 25, 2019
TodayJul 2, 2026
Enrollment to primary: 12 daysPosted 7.3 years ago
Interventions
INVSENSOR00032 and INVSENSOR00033device
Investigational pulse oximeter device