Preventing Hypoxemia With Manual Ventilation During Endotracheal Intubation (PreVent) Trial

NACompletedINTERVENTIONAL
Enrollment

401

Participants

Timeline

Start Date

March 15, 2017

Primary Completion Date

May 6, 2018

Study Completion Date

July 6, 2018

Conditions
Respiratory FailureRespiratory Failure With HypoxiaEndotracheal Intubation
Interventions
OTHER

Manual Ventilation

Beginning after the administration of sedation/neuromuscular blockade, manual ventilation will be provided by bag-valve-mask until the initiation of laryngoscopy. In patients requiring more than one attempt at laryngoscopy, bag-valve-mask ventilation will resume between laryngoscopy attempts.

OTHER

No Manual Ventilation

Between the administration of sedation/neuromuscular blockade and intubation, ventilation will not be provided unless the patient experiences an arterial oxygen saturation less than 90%. For patients who experience an oxygen saturation less than 90% after induction, bag-valve-mask ventilation may be provided.

Trial Locations (5)

35294

The University of Alabama at Birmingham, Birmingham

37209

Vanderbilt University Medical Center, Nashville

70112

Louisiana State University School of Medicine, New Orleans

70121

Ochsner Health System, New Orleans

98104

Harborview Medical Center, University of Washington, Seattle

All Listed Sponsors
lead

Vanderbilt University Medical Center

OTHER

NCT03026322 - Preventing Hypoxemia With Manual Ventilation During Endotracheal Intubation (PreVent) Trial | Biotech Hunter | Biotech Hunter