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NCT05899868 · ClinicalTrials.gov registry record · NA
Utilization of Airway Stabilizing Rod
A NA study, sponsored by Baylor College of Medicine.
- Completed
- Registry status
- NA
- Development phase
- 20
- Enrollment target
NCT05899868 is a NA study that has completed, run by Baylor College of Medicine. The registered enrollment target is 20 participants.
The verdict
NCT05899868, a NA study, has completed, sponsored by Baylor College of Medicine.
- COMPLETED
- Registry status
- NA
- Development phase
- 20 participants
- Enrollment target
Study Summary
The pediatric airway is known to be more challenging than the adult airway when performing endotracheal intubation. When a patient cannot be ventilated and/or intubated, the guidelines for airway management dictate that a laryngeal mask airway (LMA) be used as a rescue device to oxygenate and ventilate the patient. While an excellent device the LMA is seen as temporary and ultimately needs to be replaced by an endotracheal tube (ETT).
Interventions
- DEVICE Time to Intubation using FASTER device
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2023-10-12 |
| Est. Completion | 2024-05-17 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05899868
The ClinicalTrials.gov registry entry for NCT05899868 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Baylor College of Medicine, which has 616 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Time to Intubation using FASTER device is the first listed.
NCT05899868 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT05899868 about?
NCT05899868 is a clinical study titled "Utilization of Airway Stabilizing Rod". The pediatric airway is known to be more challenging than the adult airway when performing endotracheal intubation. When a patient cannot be ventilated and/or intubated, the guidelines for airway management dictate that a laryngeal mask airway (LMA) be used as a rescue device to oxygenate and ventil...
What is the current status of trial NCT05899868?
This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2023-10-12. Estimated completion is 2024-05-17.
What interventions are being tested in trial NCT05899868?
The interventions under investigation include: Time to Intubation using FASTER device (DEVICE).
Who is sponsoring clinical trial NCT05899868?
This trial is sponsored by Baylor College of Medicine, which has 616 total clinical trials registered on ClinicalTrials.gov.
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