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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: Completed NA study of Oral Intubation, sponsored by University of Maryland, Baltimore.
NCT01235065 is a NA study of Oral Intubation that has completed, run by University of Maryland, Baltimore. The registered enrollment target is 623 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (56% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
Assessment of whether or not the patient was discharged alive from the study center
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 |
What the finished NCT01235065 record still lists
NCT01235065 is an interventional study that assigns participants to a tested intervention. The registered 623 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (56% lower).
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 a single indexed study location in 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.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01235065's enrollment target sits among peer trials
623 161st of 2000 higher than 1,840 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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