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NCT01235065 · ClinicalTrials.gov registry record · NA
GlideScope Versus Direct Laryngoscope for Emergency Intubation
A NA study of Oral Intubation, sponsored by University of Maryland, Baltimore.
- Completed
- Registry status
- NA
- Development phase
- 623
- Enrollment target
- 1
- Study location
NCT01235065 is a NA study of Oral Intubation that has completed, run by University of Maryland, Baltimore. The registered enrollment target is 623 participants. The trial reports 1 study location across 1 state.
The verdict
NCT01235065, a NA study of Oral Intubation, has completed, sponsored by University of Maryland, Baltimore.
- COMPLETED
- Registry status
- NA
- Development phase
- 623 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to assess if the GlideScope video laryngoscope is superior to the Macintosh direct laryngoscope for definitive airway management in acutely-injured patients.
Conditions Studied
Interventions
- DEVICE type of laryngoscope
Study Locations (1)
Maryland
- R Adams Cowley Shock Trauma Center - Baltimore
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 623 participants |
| Start Date | 2008-07 |
| Est. Completion | 2016-11-16 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01235065
The ClinicalTrials.gov registry entry for NCT01235065 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 623 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Maryland, Baltimore, which has 560 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Oral Intubation appearing as the primary indexed condition, and to 1 intervention - of which type of laryngoscope is the first listed.
NCT01235065 reports 1 study location spanning 1 distinct geographic area - top geographies include Maryland.
Frequently Asked Questions
What is clinical trial NCT01235065 about?
NCT01235065 is a clinical study titled "GlideScope Versus Direct Laryngoscope for Emergency Intubation". The purpose of this study is to assess if the GlideScope video laryngoscope is superior to the Macintosh direct laryngoscope for definitive airway management in acutely-injured patients.
What is the current status of trial NCT01235065?
This trial is currently completed. It is a NA study. The enrollment target is 623 participants. The study started on 2008-07. Estimated completion is 2016-11-16.
What conditions does trial NCT01235065 study?
This clinical trial studies the following conditions: Oral Intubation.
What interventions are being tested in trial NCT01235065?
The interventions under investigation include: type of laryngoscope (DEVICE).
Who is sponsoring clinical trial NCT01235065?
This trial is sponsored by University of Maryland, Baltimore, which has 560 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01235065 being conducted?
This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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