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NCT01113723 · ClinicalTrials.gov registry record · Phase 4
Intubation of Patients With an Unstable Cervical Spine Using the CMAC Device
A Phase 4 study, sponsored by Cedars-Sinai Medical Center.
- Completed
- Registry status
- Phase 4
- Development phase
- 140
- Enrollment target
NCT01113723: Completed Phase 4 study, sponsored by Cedars-Sinai Medical Center.
NCT01113723 is a Phase 4 study that has completed, run by Cedars-Sinai Medical Center. The registered enrollment target is 140 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (73% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01113723, a Phase 4 study, has completed, sponsored by Cedars-Sinai Medical Center.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 140 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate whether tracheal intubation with the CMAC device decreases the time required for intubation as compared to intubation with the fiberoptic bronchoscope in patients with an unstable cervical spine. Both the CMAC device and the fiberoptic bronchoscope are currently commonly used in standard of care practices in the intubation of patients with cervical spine injury.
Primary Outcome
Times (seconds) following initial insertion of laryngoscope blade to placement of tracheal tube
Interventions
- DEVICE Fiberoptic bronchoscope
- DEVICE CMAC
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 140 participants |
| Start Date | 2009-12 |
| Est. Completion | 2012-02 |
| Phase | Phase 4 |
What the finished NCT01113723 record still lists
NCT01113723 is an interventional study that assigns participants to a tested intervention. The registered 140 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (73% lower).
The record links to 0 conditions, and to 2 interventions - of which Fiberoptic bronchoscope is the first listed.
NCT01113723 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01113723 about?
NCT01113723 is a clinical study titled "Intubation of Patients With an Unstable Cervical Spine Using the CMAC Device". The purpose of this study is to evaluate whether tracheal intubation with the CMAC device decreases the time required for intubation as compared to intubation with the fiberoptic bronchoscope in patients with an unstable cervical spine. Both the CMAC device and the fiberoptic bronchoscope are curren...
What is the current status of trial NCT01113723?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 140 participants. The study started on 2009-12. Estimated completion is 2012-02.
What interventions are being tested in trial NCT01113723?
The interventions under investigation include: Fiberoptic bronchoscope (DEVICE), CMAC (DEVICE).
Who is sponsoring clinical trial NCT01113723?
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 NCT01113723's enrollment target sits among peer trials
140 581st of 2000 higher than 1,408 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 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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