Cervical Spine Motion During Tracheal Intubation: Video Laryngoscope vs Rigid Video Stylet

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

22 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-07-25

Study Completion Date

2017-10-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

In this study, investigators are going to compare cervical spine motion during tracheal intubation using video laryngoscope or rigid video stylet in patients with simulated cervical immobilization.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Intubation Success Rate_Rigid Video Stylet Vs Video Laryngoscope

NCT02769221

Intubation, Intratracheal

UNKNOWN NA

C-MAC Videolaryngoscope Intubation and Cervical Spine Motion

NCT03567902

Intubation;Difficult Cervical Spinal Cord Injury

UNKNOWN NA

Tracheal Intubation Using Videolaryngoscope vs Fiberoptic Bronchoscope in Patients With Cervical Immobilization

NCT03759561

Intubation, Intratracheal

COMPLETED NA

Laryngoscope-assisted Lightwand Intubation and Cervical Spine Motion

NCT02430415

Intubation; Difficult

UNKNOWN NA

Optimal Intubating Technique Using Videolaryngoscopy in Patients With Semi-rigid Neck Collar

NCT04578119

Cervical Spine Surgery Intubation;Difficult

COMPLETED NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

In patients with an unstable cervical spine, neck extension during tracheal intubation may result in harmful events such as spinal cord injury. Thus, it is important to minimize cervical spine motion in these patients. In this randomized crossover study, investigators are going to compare cervical spine motion during tracheal intubation using video laryngoscope or rigid video stylet in patients with simulated cervical immobilization.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Intubation

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

OTHER

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Group A

rigid video stylet intubation - video laryngoscope intubation

Group Type EXPERIMENTAL

rigid video stylet intubation

Intervention Type DEVICE

intubation using rigid video stylet

video laryngoscope intubation

Intervention Type DEVICE

intubation using video laryngoscope

Group B

video laryngoscope intubation - rigid video stylet intubation

Group Type EXPERIMENTAL

rigid video stylet intubation

Intervention Type DEVICE

intubation using rigid video stylet

video laryngoscope intubation

Intervention Type DEVICE

intubation using video laryngoscope

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

rigid video stylet intubation

intubation using rigid video stylet

Intervention Type DEVICE

video laryngoscope intubation

intubation using video laryngoscope

Intervention Type DEVICE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Patients aged 18-80 years undergoing elective endovascular cerebral aneurysm coiling to general anesthesia in a neuroangiography suite

Exclusion Criteria

* Patients with upper airway abnormalities such as inflammation, abscesses, tumors, polyps, and trauma
* Patients with a medical history of gastroesophageal reflux disease and previous airway surgery, at high risk for aspiration, coagulation disorders, or a Hunt Hess grade of 3-5

Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No