NCT07612995

Brief Summary

The objective of this project is to develop a tracheal intubation teaching curriculum covering both normal and difficult airways using CT three-dimensional imaging and 3D printing technologies, enabling trainees to intuitively learn anatomical knowledge, operational skills, and special handling techniques, and to evaluate the learning outcomes. The research content includes the establishment of airway models and the training of students. Trainees in Group A will be trained using the tracheal intubation curriculum independently developed in this project, while trainees in Group B will be trained using traditional teaching methods, where instructors explain the course content via PowerPoint, elaborate on key and difficult points, answer student questions, and provide a summary. The teaching content for both groups is identical. After the teaching session, the teaching effectiveness will be evaluated using the second part of the teaching assessment methods.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
1mo left

Started May 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress49%
May 2026Aug 2026

First Submitted

Initial submission to the registry

April 29, 2026

Completed
2 days until next milestone

Study Start

First participant enrolled

May 1, 2026

Completed
28 days until next milestone

First Posted

Study publicly available on registry

May 29, 2026

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2026

Last Updated

May 29, 2026

Status Verified

May 1, 2026

Enrollment Period

2 months

First QC Date

April 29, 2026

Last Update Submit

May 21, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • success rate of endotracheal intubation

    fter inserting the video laryngoscope into the oral cavity, insert the endotracheal tube into the trachea.

    through study completion, an average of 1 year

Secondary Outcomes (1)

  • Complications of tracheal intubation, student satisfaction and confidence scores

    through study completion, an average of 1 year

Study Arms (2)

traditional teaching group

ACTIVE COMPARATOR

trained using traditional teaching methods, involving explanations by instructors via PowerPoint, det elaboration on key and difficult points, answering student questions, and summarizing the content.

Behavioral: the course training- traditional

the course training group

EXPERIMENTAL

trained using a tracheal intubation course independently developed for this project。

Behavioral: the course training-3D

Interventions

The experimental group received training using the curriculum developed in this study. After training, both groups performed tracheal intubation on patients, and thon operation scores, as well as the satisfaction of students and teachers, were evaluated

the course training group

Vtrained using traditional teaching methods, involving explanations by instructors via PowerPoint, det elaboration on key and difficult points, answering student questions, and summarizing the content

traditional teaching group

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • The only patients who were selected for the intubation were grade I and II according to the American Society of Anesthesiologists (ASA), non-obese and with good visualization of soft palate and uvula (Mallampati classification)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Shanxibaiqiuen Hospital

Taiyuan, Shaanxi, 030000, China

RECRUITING

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
principal investigator

Study Record Dates

First Submitted

April 29, 2026

First Posted

May 29, 2026

Study Start

May 1, 2026

Primary Completion (Estimated)

July 1, 2026

Study Completion (Estimated)

August 1, 2026

Last Updated

May 29, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will not share

Locations