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NCT05327842 Clinical Trial

Evaluation of a Flexible Videoscope Training Simulator

Difficult Airway Clinical Trial

Official title:
Evaluation of a Flexible Videoscope Training Simulator: a Randomized, Controlled, Simulation Teaching Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05327842
Other study ID # TJMZK220405
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 15, 2022
Est. completion date July 2, 2022

Study information
Verified date July 2022
Source Tongji Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Flexible bronchoscope or videoscope plays important roles in managing difficult airway. But this technique is time-consuming and very difficult to learn for novices. The investigators design a simple training simulator to help them master this technique.

Description:

In this study, residents without operational experience will be recruited. The training effect of the new simulator will be evaluated by comparison with traditional simulation teaching. Participants will receive training with the new simulator or traditional method for 1hour, and then they perform intubation with flexible videoscope in a simulated difficult airway model. The insertion time and success rate will be recorded. Last, they will complete the questionnaire.

Recruitment information / eligibility
Status Completed
Enrollment 43
Est. completion date July 2, 2022
Est. primary completion date June 30, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Resident or Medical student - Willing to participate to the study - Consent to evaluate the measured data Exclusion Criteria: - experienced anesthetists

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• New training simulator
Participants receive training with new simulator
• Traditional simulator
Participants receive traditional training

Locations
Country Name City State
China Department of Anesthesiology, Tongji Hospital Wuhan Hubei

Sponsors (1)
Lead Sponsor Collaborator
Tongji Hospital

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Other Questionnaire A questionnaire was used to measure the self-evaluation of the trained persons 1 hour
Primary insertion time time when participants perform flexible videoscope from incisor to carina 1 hour
Secondary success rate the rate of participants used flexible videoscope to view carina successfully 1 hour
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