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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.

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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

FieldValue
Enrollment Target 140 participants
Start Date 2009-12
Est. Completion 2012-02
Phase Phase 4

Sponsor

Cedars-Sinai Medical Center

339 total trials

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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.