Actively Recruiting

Phase Not Applicable
All Genders
Healthy Volunteers
ID07612995

Impact of CT-based 3D Models and 3D Printing Technology on Success Rate in Endotracheal Intubation in Undergraduate Medical Students A Prospective Single-Center Study

Led by xiaojing wang · Updated on 2026-05-29

80

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to develop and evaluate a teaching curriculum for tracheal intubation using CT-based three-dimensional imaging and 3D printing technologies. The goal is to help students learn anatomical knowledge, operational skills, and special handling techniques for both normal and difficult airways. The study compares this new curriculum with traditional teaching methods to assess their relative effectiveness. Participants are divided into two groups. Group A receives training with the newly developed 3D curriculum, while Group B is trained using traditional teaching, which involves instructors explaining the material via PowerPoint, highlighting key points, answering questions, and summarizing the content. Both groups cover the same teaching content. After training, students perform tracheal intubation on patients. During the study, researchers will evaluate the success rate of endotracheal intubation over approximately one year. Additional outcomes include complications related to intubation and student satisfaction and confidence scores. The study monitors the participants' performance, satisfaction, and training outcomes to compare the two teaching methods effectively.

CONDITIONS

Brief Title

Impact of Via CT-based 3D Printing Technology on Success Rate in Endotracheal Intubation in Students

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients selected for intubation must be classified as American Society of Anesthesiologists (ASA) grade I or II
  • Patients must be non-obese
  • Patients must have good visualization of the soft palate and uvula according to Mallampati classification
Not Eligible

You will not qualify if you...

  • No exclusion criteria specified

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - Up to 1 year

Participants receive training using either the traditional teaching methods or the specially developed tracheal intubation course. After training, they perform endotracheal intubation on patients to assess skills and satisfaction.

Training and assessment sessions scheduled as per group assignment

Trial Site Locations

Total: 1 location

1

Shanxibaiqiuen Hospital

Taiyuan, Shaanxi, China, 030000

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Research Team

X

xiaojing wang

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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