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

NCT ID: NCT01129726

Last Updated: 2012-02-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2010-05-31

Study Completion Date

2011-12-31

Brief Summary

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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.

Detailed Description

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Conditions

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Transillumination-guided Fiberoptic Intubation Intubation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

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Intubation

Transillumination-guided Fiberoptic Intubation

Group Type EXPERIMENTAL

Transillumination-guided Fiberoptic Intubation

Intervention Type DEVICE

Light guided, Non-invasive

Interventions

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Transillumination-guided Fiberoptic Intubation

Light guided, Non-invasive

Intervention Type DEVICE

Other Intervention Names

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Light guided Bronchoscopic Intubation Technique

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Second Military Medical University

OTHER

Sponsor Role lead

Responsible Party

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Yang Tao

Department of Anesthesiology and Cirtical Care Medicine, Changhai Hospital

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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XiaoMing Deng, Ph.D.

Role: STUDY_CHAIR

Second Military Medical University

Locations

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Changhai Hospital Affiliated to Second Military Medical University

Shanghai, Shanghai Municipality, China

Site Status

Changhai Hospital affiliated to Second Military Medical University

Shanghai, , China

Site Status

Countries

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China

Other Identifiers

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Light Guided

Identifier Type: OTHER

Identifier Source: secondary_id

20100002

Identifier Type: -

Identifier Source: org_study_id

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