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Device
Video Laryngoscopy for Pyloric Stenosis
N/A
Waitlist Available
Led By Nicole Horn, MD
Research Sponsored by Indiana University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Need general anesthesia for pyloromyotomy procedure
Be younger than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up during intubation attempt (less than two minutes)
Awards & highlights
Study Summary
This trial is comparing two ways to place breathing tubes for surgery in infants with pyloric stenosis.
Eligible Conditions
- Pyloric Stenosis
- Pediatric Intubation
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
You require general anesthesia for a surgical procedure called pyloromyotomy.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ during intubation attempt (less than two minutes)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~during intubation attempt (less than two minutes)
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Number of Participants Who Had Desaturation Below 80% During Intubation
Trial Design
2Treatment groups
Active Control
Group I: Conventional Direct LaryngoscopyActive Control1 Intervention
Endotracheal intubation will be performed by conventional direct laryngoscopy.
Group II: Video LaryngoscopyActive Control1 Intervention
Endotracheal intubation will be performed by video laryngoscopy with the C-MAC.
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Who is running the clinical trial?
Indiana UniversityLead Sponsor
976 Previous Clinical Trials
983,315 Total Patients Enrolled
Nicole Horn, MDPrincipal InvestigatorSponsor-Investigator
1 Previous Clinical Trials
100 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You have a problem with your airway that makes it difficult for you to breathe.You require general anesthesia for a surgical procedure called pyloromyotomy.You are allergic to succinylcholine and/or propofol.
Research Study Groups:
This trial has the following groups:- Group 1: Conventional Direct Laryngoscopy
- Group 2: Video 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.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are new participants currently being enrolled in this experiment?
"Clinicaltrials.gov does not show that this study is currently enlisting participants; it was first posted on September 1st 2013 and its most recent edit occurred on August 19th 2022. Nevertheless, there are 7 separate trials with open recruitment at the moment."
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