AI-based Prediction Model of Difficult Tracheal Intubation Using Medical Image Parameters
NCT ID: NCT06982144
Last Updated: 2025-05-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
228 participants
OBSERVATIONAL
2025-05-20
2026-05-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
THE ROLE OF ARTIFICIAL INTELLIGENCE TRAINED WITH PRE-MEASURED NUMERICAL DATA IN PREDICTION OF DIFFICULT INTUBATION
NCT06961240
A Predictive Model for Difficult Intubation
NCT02944305
Evaluation of Double Lumen Tube Intubation Difficulty With Photo-Based Artificial Intelligence Algorithms
NCT06839261
Anthropometric and US-Guided Difficult Intubation Prediction With ML Models
NCT06904586
Comparison of Two Bending Angles for Nasotracheal Intubation With a Malleable Vedio Stylet
NCT04459481
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Adult patients scheduled for selective surgery
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. surgical patients undergoing general anesthesia with endotracheal intubation;
3. with head and neck CT examination results
4. Consent to participate in the study.
Exclusion Criteria
2. The presence of airway stenosis, including internal airway stenosis (such as foreign body or tumor) or stenosis caused by external tracheal mass compression;
3. tracheo-esophageal fistula;
4. severe gastroesophageal reflux;
5. previous upper airway surgery, such as laryngeal cancer radical surgery, snoring surgery, etc.
6)participating in other research projects
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Mu Dong Liang
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Mu Dong Liang
Professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Peking University First Hospital
Beijing, Beijing Municipality, China
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2025R-0037
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.