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A Bidirectional Cohort Study on the Establishment of a Nutrition-Inflammation Burden Assessment System and Prognostic Prediction Model for Oral Squamous Cell Carcinoma

A Bidirectional Cohort Study on the Establishment of a Nutrition-Inflammation Burden Assessment System and Prognostic Prediction Model for Oral Squamous Cell Carcinoma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400088053
Enrollment
Unknown
Registered
2024-08-09
Start date
2024-08-09
Completion date
Unknown
Last updated
2024-08-12

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

prospective cohort:None
retrospective cohort:None

Sponsors

Beijing Stomatological Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Age: 18 years old or above (including 18 years old); (2) Gender: male or female; (3) The primary first-time patient, preoperative or postoperative pathologically confirmed to be squamous cell carcinoma; (4) Tumor site: lips, tongue, buccal mucosa, upper and lower gingiva (including posterior molars), floor of the mouth, hard palate mucosa; (5) Clinical stage: cT1-4N0-3M0 (based on clinical examination, contrast-enhanced CT/MRI); (6) Radical surgery for oral cancer in our hospital; The systemic condition can tolerate the treatment regimen, there are no contraindications to surgery, distant metastases are excluded by chest x-ray and/or abdominal ultrasound, and CT and/or MRI and/or PET/CT with contrast in suspicious cases to assist in diagnosis.

Exclusion criteria

Exclusion criteria: (1) Clinical case data cannot be obtained; (2) Missing values of key variables of nutrient/inflammatory burden; (3) pregnant or lactating women; (4) Those with mental disorder or intellectual disability are expected to be unable to complete treatment and follow-up.

Design outcomes

Primary

MeasureTime frame
3-year Disease-specific survival rate;

Secondary

MeasureTime frame
Over-all survival ;Disease-free survival;incidence of postoperative complications;

Countries

China

Contacts

Public ContactWang Chong

Beijing Stomatological Hospital, Capital Medical University

375530313@qq.com+86 138 1026 1903

Outcome results

None listed

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