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Fiberoptic Intubation and Transillumination-guided Fiberoptic Intubation:Success Rate and Time in Untrained Medical Personnel

Fiberoptic Intubation and Transillumination-guided Fiberoptic Intubation:Time and Success Rate in Untrained Medical Personnel

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01129726
Enrollment
100
Registered
2010-05-25
Start date
2010-05-31
Completion date
2011-12-31
Last updated
2012-02-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Transillumination-guided Fiberoptic Intubation Intubation

Keywords

Transillumination-guided, Fiberoptic Intubation, time, success rate, intubation

Brief summary

Fiberoptic Intubation is the preferred technique to difficult airway. However, when performed by untrained anesthesiologists, bronchoscopic intubation has a high rate of failure. We want to know if the Transillumination-guided Fiberoptic Intubation technique can improves the success rate and time for tracheal intubation performed by inexperienced anesthesiologists; whether this technique improves the success rate and for normal intubations when performed by inexperienced anesthesiologists as well is unknown. Therefore, the authors compared the success rate and time of Fiberoptic Intubation versus the Transillumination-guided Fiberoptic Intubation performed by anesthesiologists inexperienced in Fiberoptic Intubation.

Interventions

DEVICETransillumination-guided Fiberoptic Intubation

Light guided, Non-invasive

Sponsors

Second Military Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* general anesthesia * ASA I\ II * Mallampati Score grade I\ II * thyromental distance ≥6cm * mouth-open ≥3cm * body mass index (BMI) ≤30kg/m2

Exclusion criteria

* neck and maxillofacial surgeries * potential risks for regurgitation and pulmonary aspiration * in pregnancy

Design outcomes

Primary

MeasureTime frame
time to intubationWithin 3 month

Secondary

MeasureTime frame
success rate and postoperative side effect2 months

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026