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NCT01371032 · ClinicalTrials.gov registry record · NA
Study: Study to Compare Video Miller Device to Direct Laryngoscopy
A NA study, sponsored by Cedars-Sinai Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 28
- Enrollment target
NCT01371032: Completed NA study, sponsored by Cedars-Sinai Medical Center.
NCT01371032 is a NA study that has completed, run by Cedars-Sinai Medical Center. The registered enrollment target is 28 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01371032, a NA study, has completed, sponsored by Cedars-Sinai Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 28 participants
- Enrollment target
Study Summary
The purpose of this study is to compare: the standard pediatric intubation instrument (Miller blade) used as direct laryngoscopy during tracheal intubation to the VideoMiller device (the standard pediatric blade with a camera attached, giving indirect view of the vocal cords in the screen). This intubation device is used to place the tube in the trachea to keep the patient breathing during the surgery procedure. The anesthesiologist obtains a better view of the vocal cords looking at the screen provided by the VideoMiller.
Primary Outcome
Time to obtain glottic view (from initial insertion of laryngoscope blade to obtain glottic view)
Interventions
- DEVICE Direct Laryngoscopy
- DEVICE VideoMiller
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 28 participants |
| Start Date | 2011-06 |
| Est. Completion | 2015-12 |
| Phase | NA |
What the finished NCT01371032 record still lists
NCT01371032 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 28 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).
The record links to 0 conditions, and to 2 interventions - of which Direct Laryngoscopy is the first listed.
NCT01371032 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01371032 about?
NCT01371032 is a clinical study titled "Study: Study to Compare Video Miller Device to Direct Laryngoscopy". The purpose of this study is to compare: the standard pediatric intubation instrument (Miller blade) used as direct laryngoscopy during tracheal intubation to the VideoMiller device (the standard pediatric blade with a camera attached, giving indirect view of the vocal cords in the screen). This in...
What is the current status of trial NCT01371032?
This trial is currently completed. It is a NA study. The enrollment target is 28 participants. The study started on 2011-06. Estimated completion is 2015-12.
What interventions are being tested in trial NCT01371032?
The interventions under investigation include: Direct Laryngoscopy (DEVICE), VideoMiller (DEVICE).
Who is sponsoring clinical trial NCT01371032?
This trial is sponsored by Cedars-Sinai Medical Center, which has 339 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01371032's enrollment target sits among peer trials
28 1704th of 2000 higher than 293 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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