Clinical trial · Observational
GlideScope Spectrum Video Laryngoscope Blades and Stylet for Use in Neonate & Pre-Adolescent Populations
Assessment of the GlideScope Spectrum Video Laryngoscope Blades and Stylet for Use in Neonate & Pre-Adolescent Populations: Pilot Manikin Study
NCT04836338CI-TRIAL-00051109completedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The overall purpose of this study is to assess the functionality \& impact of the use of the newly designed GlideScope Spectrum pediatric video laryngoscope and stylet for the orotracheal intubation of neonates and pediatric patients, utilizing manikin models.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Pediatric ALL | Childhood Acute Lymphoblastic Leukemia | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| orotracheal intubation | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- Participants
- description
- Anesthesia and emergency medicine providers who perform pediatric orotracheal intubations
- interventionNames
- Device: orotracheal intubation
Primary outcomes (3)
- measure
- Time to intubate
- timeFrame
- 120 seconds - This is the maximum time allowed. After this time, it will be recorded as a failed attempt.
- description
- Time to intubate on each of 3 attempts per blade, on each manikin type.
- measure
- First pass success rate
- timeFrame
- 120 seconds - This is the maximum time allowed. After this time, it will be recorded as a failed attempt.
- description
- First pass success rate on each of 3 attempts per blade, on each manikin type. First pass success (FPS) is defined as the ability to place a tracheal tube below a patient's vocal cords on the first attempt without removing the video laryngoscope from the patient's mouth.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Anesthesia and emergency medicine providers who perform pediatric orotracheal intubations * Able to give voluntary consent to participate in the study * Are experienced with orotracheal intubation (\> 50 times) using direct laryngoscopy or video laryngoscopy Exclusion Criteria: * Volunteers who are \< 18 years of age * Volunteers unable to read or understand English * Unable to physically meet the demands of orotracheal intubation or those who have heart, wrist, or low back disease. Are not experienced with pediatric orotracheal intubations
References
Publications (0)
Data not yet available
No reference posted for this study.