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Research and development and verification of an intelligent diagnosis system for oral squamous cell carcinoma based on gas detection

Research and development and verification of an intelligent diagnosis system for oral squamous cell carcinoma based on gas detection

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500109977
Enrollment
Unknown
Registered
2025-09-28
Start date
2024-07-09
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

Oral squamous cell carcinoma

Interventions

OSCC Group:None
Healthy Group:None

Sponsors

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Experimental Group: (1) Be 18 years of age or older; (2) No gender restrictions; (3) Treatment Stage: Patients diagnosed with oral squamous cell carcinoma who have not previously received or are currently undergoing radiotherapy and chemotherapy; (4) Diagnostic Group: Patients with a confirmed pathological diagnosis of oral squamous cell carcinoma; (5) Screening Group: High-risk population for oral squamous cell carcinoma, including: 1) Patients diagnosed with oral leukoplakia or erythroplasia; 2) Individuals with a family history or genetic predisposition to oral squamous cell carcinoma; 3) Patients with long-term exposure (10 years or more) to known carcinogens such as tobacco, alcohol, or betel nuts; 4) Patients with oral lesions highly suspicious of malignancy but not yet diagnosed. Healthy Control Group: (1) Be 18 years of age or older; (2) No gender restrictions; (3) No history or current diagnosis of oral squamous cell carcinoma.

Exclusion criteria

Exclusion criteria: (1) Patients with malignant tumors in other parts of the body; (2) Patients who have already participated in other clinical studies; (3) Patients with severe mental illness or cognitive impairment who are unable to understand and comply with the research requirements; (4) Patients who are undergoing drug treatment that may affect the research results (such as antibiotics and anti-inflammatory drugs) and are unable to stop taking the medication; (5) Patients with drug abuse or alcoholism that affects their compliance with the study; (6) Patients who are not suitable to participate in this study as stipulated by law or ethics; (7) Patients who the researcher deems unsuitable for inclusion in the study (such as those with other factors that may affect the study results).

Design outcomes

Primary

MeasureTime frame
Oral exhaled gas metabolomics;

Secondary

MeasureTime frame
saliva metagenomics;

Countries

China

Contacts

Public ContactJiannan Liu

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine

laurence_ljn@163.com+86 21 2327 1699

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026