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Comparison of the VividTrac® Videolaryngoscope to Direct Laryngoscopy in Adults Under Manual Inline Stabilization

Comparison of the VividTrac® Videolaryngoscope to Direct Laryngoscopy in Adults Under Manual Inline Stabilization

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02479672
Enrollment
0
Registered
2015-06-24
Start date
2016-01-31
Completion date
2016-07-31
Last updated
2016-10-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endotracheal Intubation

Keywords

breathing tube placement, VideoTrac® laryngoscope, direct laryngoscopy

Brief summary

This is a prospective randomized clinical study to be performed in adult patients ages 18 and older who are undergoing surgical procedures requiring endotracheal intubation. Adult patients will be randomized to either the VideoTrac® laryngoscope or direct laryngoscopy and the time to intubation will be compared and recorded. Patients in both treatment arms will receive manual inline stabilization. The study hypothesis is that the time to endotracheal intubation will be decreased in the VividTrac® video laryngoscope group when compared to direct laryngoscopy.

Interventions

DEVICElaryngoscopy

Placement of endotracheal tube. If successful intubation does not occur after the first attempt at laryngoscopy, airway equipment used in further attempts will be selected at the discretion of the attending anesthesiologist.

PROCEDUREManual Inline Stabilization

Manual immobilization of Patient's neck with intention to minimize movement from baseline position

DEVICEVividTrac®

Sponsors

Loma Linda University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients will be 18 years old and older requiring endotracheal intubation

Exclusion criteria

* Patients with increased pulmonary risk; * Prior documentation of difficult endotracheal intubation; * elevated intracranial pressure; * those who lack legal representative consent

Design outcomes

Primary

MeasureTime frameDescription
Time to Intubationday of surgeryTime frame being assessed will begin at the time of mouth opening and end with the removal of the tip of laryngoscope blade from the patient's mouth after successful endotracheal intubation.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026