At a glance
ClinicalIndex Comparison RecordN/ACompleted· 29 enrolled
Drug / intervention
Noninvasive Ventilator (V60, Philips)device
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.
Electric Blower Based Ventilator Used During Procedural Sedation
In Brief
A clinical study evaluating Noninvasive Ventilator (V60, Philips) for Apnea During Procedural Sedation. Completed, enrolled 29 participants.
Detailed Summary
Conduct human trials in the endoscopy suite of our continuous positive airway pressure (CPAP) ventilator approach using an FDA approved ventilator.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsApnea During Procedural Sedation
Countries--
CollaboratorsNational Aeronautics and Space Administration (NASA)
Timeline
N/ACompletedFinished
20162017201820192020202120222023202420252026
Enrollment StartDec 2015
First PostedDec 2015
Primary CompletionJun 2019
TodayJul 2026
First PostedDec 3, 2015
Enrollment StartDec 1, 2015
Primary CompletionJun 1, 2019
TodayJul 2, 2026
Enrollment to primary: 3.5 yearsPosted 10.6 years ago
Interventions
Noninvasive Ventilator (V60, Philips)device
The clinician will determine the concentration of oxygen that shall be delivered to the patient. The ventilator is capable of providing concentrations between 21% - 100% of oxygen. Unless otherwise directed by the clinician, the default setting of 40% will be used.