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Videolaryngoscopy vs. Direct Laryngoscopy for Intubation
N/A
Waitlist Available
Led By Kurt Ruetzler, MD
Research Sponsored by The Cleveland Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from the start time of intubation to time of the end of surgery up to 45 minutes
Awards & highlights
Study Summary
This trial will compare how successful intubation is when performed with a video laryngoscope vs. a conventional direct laryngoscope, in terms of both number of intubation attempts and airway trauma.
Who is the study for?
This trial is for patients who need a tube placed in their windpipe through the mouth for general anesthesia during elective or emergency surgery. It's not suitable for cases where the anesthesiologist recommends a specific method, or when awake fiberoptic intubation or double-lumen tubes are needed.Check my eligibility
What is being tested?
The study compares two ways to place a breathing tube: using a GlideScope videolaryngoscope (a device with a camera) versus the traditional direct laryngoscopy without video assistance. The goal is to see which method has higher success on the first try and causes less injury.See study design
What are the potential side effects?
Potential side effects may include sore throat, difficulty swallowing, hoarseness, and minor oral or airway injuries. These can result from either technique used in placing the breathing tube.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ from the start time of intubation to time of the end of surgery up to 45 minutes
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from the start time of intubation to time of the end of surgery up to 45 minutes
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
The number of intubation attempts with the initial laryngoscopy instrument.
Secondary outcome measures
Any dental or airway injury
Intubation failure
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: videolaryngoscopyExperimental Treatment1 Intervention
Initial intubation performed using GlideScope videolaryngoscope.
Group II: conventional direct laryngoscopyActive Control1 Intervention
Initial intubation performed using direct laryngoscopy.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
GlideScope videolaryngoscope (Verathon, Bothell, WA 98011)
2021
N/A
~12710
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Video laryngoscopy enhances the visualization of the airway by using a camera and a video screen, which allows for a clearer and more detailed view compared to conventional direct laryngoscopy. This improved visualization can lead to higher success rates in intubation, fewer attempts needed, and reduced airway trauma.
For patients, this means a potentially safer procedure with fewer complications and a higher likelihood of successful intubation on the first attempt, which is crucial in emergency and surgical settings.
Airway evaluation in obstructive sleep apnea.
Airway evaluation in obstructive sleep apnea.
Find a Location
Who is running the clinical trial?
The Cleveland ClinicLead Sponsor
1,034 Previous Clinical Trials
1,352,724 Total Patients Enrolled
Kurt Ruetzler, MDPrincipal InvestigatorThe Cleveland Clinic
4 Previous Clinical Trials
1,209 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- The medical team needs to perform a special type of breathing tube procedure while you are awake.You have a double-lumen tube inserted.
Research Study Groups:
This trial has the following groups:- Group 1: videolaryngoscopy
- Group 2: conventional direct laryngoscopy
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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