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NCT01091948 · ClinicalTrials.gov registry record · NA
GlideScope Video Laryngoscope Versus Fiberoptic Intubation
A NA study, sponsored by The Cleveland Clinic.
- Completed
- Registry status
- NA
- Development phase
- 75
- Enrollment target
NCT01091948 is a NA study that has completed, run by The Cleveland Clinic. The registered enrollment target is 75 participants.
The verdict
NCT01091948, a NA study, has completed, sponsored by The Cleveland Clinic.
- COMPLETED
- Registry status
- NA
- Development phase
- 75 participants
- Enrollment target
Study Summary
Following informed consent, patients will be randomly assigned to oral fiberoptic intubation or to oral intubation using the GlideScope Video Laryngoscope. Following the induction of general anesthesia a sealed envelope would be opened to reveal the technique to be used. A stop watch will be started at the beginning of the procedure. At the completion of intubation the stop watch will be stopped and the time recorded along with other data. Based on a sample size estimation process, it is the investigators plan to study fifty patients. The two techniques will be compared in terms of the average time needed to place the endotracheal tube and studied using a two-sided T-Test with a significance level of 0.05. To ensure comparability between the two methods, all intubators will be required to have at experienced at least 10 uses of the GlideScope and 10 uses with fiberoptic intubation.
Interventions
- DEVICE Intubation with Fiberoptic laryngoscope
- DEVICE GlideScope® Video Laryngoscope
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 75 participants |
| Start Date | 2008-02 |
| Est. Completion | 2010-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01091948
The ClinicalTrials.gov registry entry for NCT01091948 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 75 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The Cleveland Clinic, which has 688 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Intubation with Fiberoptic laryngoscope is the first listed.
NCT01091948 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01091948 about?
NCT01091948 is a clinical study titled "GlideScope Video Laryngoscope Versus Fiberoptic Intubation". Following informed consent, patients will be randomly assigned to oral fiberoptic intubation or to oral intubation using the GlideScope Video Laryngoscope. Following the induction of general anesthesia a sealed envelope would be opened to reveal the technique to be used. A stop watch will be started...
What is the current status of trial NCT01091948?
This trial is currently completed. It is a NA study. The enrollment target is 75 participants. The study started on 2008-02. Estimated completion is 2010-01.
What interventions are being tested in trial NCT01091948?
The interventions under investigation include: Intubation with Fiberoptic laryngoscope (DEVICE), GlideScope® Video Laryngoscope (DEVICE).
Who is sponsoring clinical trial NCT01091948?
This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.
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