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NCT02621463

Electric Blower Based Ventilator Used During Procedural Sedation

Completed NA Results posted Last updated 27 April 2021
What this trial tests

NA trial testing Noninvasive Ventilator (V60, Philips) in Apnea During Procedural Sedation in 29 participants. Completed in 1 June 2019.

Timeline
1 December 2015
Primary endpoint
1 June 2019
1 June 2019

Quick facts

Lead sponsorUniversity of Utah
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposesupportive care
Enrollment29
Start date1 December 2015
Primary completion1 June 2019
Estimated completion1 June 2019

Drugs / interventions tested

Conditions studied

Sponsor

University of Utah

Who can join

18 and older, any sex, with Apnea During Procedural Sedation. Patients with the condition only — healthy volunteers not accepted.

Results — posted to ClinicalTrials.gov

Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.

Percentage of Time the Patient Will Experience Apnea Primary · Duration of Diagnostic Procedure (Colonoscopy)

Length of time in minutes the patient experiences apnea divided by the length of time of the diagnostic procedure (Unit: %)

GroupValue95% CI
Noninvasive Ventilation114 – 22

Sponsor's own description

Conduct human trials in the endoscopy suite of our continuous positive airway pressure (CPAP) ventilator approach using an FDA approved ventilator.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other University of Utah trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02621463.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing