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Clinical Trials/NCT05410236
NCT05410236
Completed
Not Applicable

The Application of Three-dimensional Printing in Airway Anatomy and Bronchoscopy Education

Fu Jen Catholic University1 site in 1 country26 target enrollmentJuly 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Satisfaction, Personal
Sponsor
Fu Jen Catholic University
Enrollment
26
Locations
1
Primary Endpoint
Examination score of pre-intervention
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The main purpose of this study is to use 3D printing technology to make a human anatomical bronchial tree model, which is applied in medical education for medical students and students of the department of respiratory therapy. Most of the clinical teaching material is expansive and inaccessible. To promote accessibility of anatomy models and student learning effects in our school and hospital, we use the 3D printing technology to print bronchial tree model and apply it to anatomy and bronchoscopy education.

The present study expects some benefits that the use of printed bronchial trees for anatomy and bronchoscopy education. For example, it can reduce the cost of anatomy instruction, let students have their own anatomical model, and make the learning no longer limited to the anatomical classroom.

Detailed Description

Three-dimensional (3D) printing is a technology used for the rapid production of customized physical objects. Bronchoscopy is a well-established, relatively safe procedure for both diagnostic and therapeutic interventions for a variety of pulmonary diseases. In this study, to enhance the quality of airway anatomy education and bronchoscopy training, we used 3D printing to develop a 3D bronchial tree model as a high-fidelity simulator for bronchoscopy and demonstrated its validity. We designed a 3D bronchial tree model containing 12 detachable parts and 11 adapter rings.

Registry
clinicaltrials.gov
Start Date
July 1, 2022
End Date
December 1, 2022
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ke-Yun, Chao

Group leader of Respiratory Therapy

Fu Jen Catholic University

Eligibility Criteria

Inclusion Criteria

  • Student of Fu Jen Catholic University.

Exclusion Criteria

  • Refused to participate in the study.

Outcomes

Primary Outcomes

Examination score of pre-intervention

Time Frame: pre-intervention

score of pre-intervention (maximun 100 and minimum 0), higher means a better outcome.

Examination score of post-intervention

Time Frame: immediately after the intervention

score of post-intervention (maximun 100 and minimum 0), higher means a better outcome.

Study Sites (1)

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