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Personalized medicine research based on head and neck cancer organoid technology

Personalized medicine research based on head and neck tumor organoid technology

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300079084
Enrollment
Unknown
Registered
2023-12-25
Start date
2024-01-01
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

head and neck tumor

Interventions

Case series:None

Sponsors

Zhongshan Hospital Affiliated to Dalian University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Sign the informed consent voluntarily. Age=18, gender is not limited. ECOG score: 0-4 points. The subjects have good compliance, can comply with the procedures related to learning, and are able and willing to complete the questionnaire surveys related to their environmental/occupational exposure and smoking/drinking history. Any patient with head and neck cancer of any subtype and stage. Primary or metastatic lesions can obtain surgical tissue or sufficient biopsy tissue, which can provide tumor tissue samples for culture. Life expectancy is not less than 12 weeks. The main organs function normally, and the heart, liver, kidney, and bone marrow hematopoietic functions are good.

Exclusion criteria

Exclusion criteria: 1) Those under 18 years old. 2) History of severe neurological or psychiatric disorders, including seizures or dementia, physical or mental incapacity or inability to sign informed consent, and inability to give informed consent (language, intelligence, etc.). 3)Refusal to participate. 4)It is impossible to obtain samples such as biopsy and/or surgery, pleural effusion, ascites, pericardial effusion, and cerebrospinal fluid. 5)There is not enough head and neck tumor tissue for histological analysis or the remaining head and neck tumor tissue is not sufficient for routine pathological analysis. 6)Those who are allergic to anti-tumor drugs or have surgical contraindications and cannot receive any anti-tumor treatment. 7)Any other history of clinically active malignant tumor within the first 5 years of enrollment 8)According to the attending physician's judgment, the patient will not be able to meet the requirements of the study. 9)Serious liver disease, cardiovascular disease, kidney disease, respiratory system disease, blood system disease or out of control diabetes. 10)HIV patients. 11)Pregnant and lactating patients.

Design outcomes

Primary

MeasureTime frame
Organoid characteristics and drug sensitivity;

Countries

China

Contacts

Public ContactRuoyu Wang

Zhongshan Hospital Affiliated to Dalian University

wangruoyu1963@163.com+86 411 6289 3970

Outcome results

None listed

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