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Research on an Intelligent Diagnostic System for Glottic Laryngeal Cancer Based on Multimodal Medical Data

Research on an Intelligent Diagnostic System for Glottic Laryngeal Cancer Based on Multimodal Medical Data

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600120305
Enrollment
Unknown
Registered
2026-03-12
Start date
2025-04-18
Completion date
Unknown
Last updated
2026-03-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glottic Laryngeal Cancer

Interventions

Observation group of glottic laryngeal cancer:None

Sponsors

The First Affiliated Hospital, Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >=18 years; 2. Patients who were hospitalized in the Department of Otorhinolaryngology of our hospital for surgical treatment, and were pathologically diagnosed with glottic cancer or vocal cord dysplasia based on postoperative pathological results; 3. Preoperative electronic laryngoscopy was performed in our hospital, with an interval of no more than 1 month between the examination and the surgery; 4. Preoperative contrast-enhanced neck CT scan was performed in our hospital, with the scan range covering from the lower border of the foramen magnum to the upper border of the aortic arch, and an interval of no more than 2 months between the examination and the surgery; 5. Complete electronic medical record data; clear and complete electronic laryngoscopy image data; clear and complete venous phase images from the contrast-enhanced CT scan.

Exclusion criteria

Exclusion criteria: 1. Patients not initially diagnosed at our hospital, who have undergone laryngeal surgery related to the current admission at another institution; 2. Patients with a history of radiotherapy, chemotherapy, or targeted therapy for head and neck tumors; 3. Patients with other types of head and neck tumors involving the glottis; 4. Lesions too small or whose original morphology is indistinguishable due to (multiple) laryngeal biopsies performed prior to the CT examination; 5. Incomplete basic patient information; 6. Prospectively enrolled patients who decline to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
Area Under the Curve (AUC);

Secondary

MeasureTime frame
Accuracy;Sensitivity;Specificity;Positive Predictive Value;Negative Predictive Value;

Countries

China

Contacts

Public ContactLei Wenbin

The First Affiliated Hospital, Sun Yat-sen University

leiwb2013@aliyun.com+86 20 8775 5766

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 20, 2026