At a glance
ClinicalIndex Comparison RecordPhase 4Completed· 140 enrolled
Drug / intervention
Fiberoptic bronchoscope +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Randomized Prospective Study to Compare Tracheal Intubation With the CMAC Device to Fiberoptic Bronchoscopy in Patients With an Unstable Cervical Spine
In Brief
A Phase 4 clinical trial evaluating Fiberoptic bronchoscope and CMAC for Laminectomy. Completed, enrolled 140 participants across 1 site.
Detailed 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.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsLaminectomy
CountriesUnited States
Collaborators--
Timeline
Phase 4CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
Enrollment StartDec 2009
First PostedApr 2010
Primary CompletionFeb 2012
TodayJul 2026
First PostedApr 30, 2010
Enrollment StartDec 1, 2009
Primary CompletionFeb 1, 2012
TodayJul 2, 2026
Enrollment to primary: 2.2 yearsPosted 16.2 years ago
Interventions
Fiberoptic bronchoscopedevice
Fiberoptic bronchoscope device
CMACdevice
CMAC Device