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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 is a Phase 4 study that has completed, run by Cedars-Sinai Medical Center. The registered enrollment target is 140 participants.
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.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01113723
The ClinicalTrials.gov registry entry for NCT01113723 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 140 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cedars-Sinai Medical Center, which has 339 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Fiberoptic bronchoscope is the first listed.
NCT01113723 reports 0 study locations.
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.
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