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Recruiting Observational

"Xijiang Project" Screening Cohort for NPC

NCT06787456 · tracked via the Priya Life Science China tracker
Phase
Observational
Started
2024-11-14
Last updated
2026-09-01

Condition(s) studied

Nasopharyngeal Carcinoma (NPC)Screening

Investigational drug(s) / intervention(s)

EBV antibodies testEBV DNA testepidemiological information surveyClinical examinations for high-risk participantsEBV and human genetic sequencing

EBV antibodies test: Test for VCA-IgA, EBNA1-IgA, EA-IgA, Zta-IgA, Rta-IgG and P85-Ab in nasopharyngeal brushing and plasma in plasma, saliva and nasopharyngeal brushing.

EBV DNA test: quantitative polymerase chain reaction, methylation sequencing and target sequencing of EBV DNA in nasopharyngeal brushing, saliva and plasma.

epidemiological information survey: epidemiological information survey including basic conditions, dietary and lifestyle habits, social, geographical, environmental, and other information.

Clinical examinations for high-risk participants: nasopharyngoscopy, head and neck MRI.

EBV and human genetic sequencing: EB virus and human genetic sequencing for plasma, etc.

Study summary

The purpose of this study is to establish a comprehensive and integrated nasopharyngeal carcinoma screening cohort, which includes an epidemiological information database containing basic information, gender, age, ethnic and family history, dietary and lifestyle habits, and geographical environmental factors; a biobank of blood, tissue fluid, swabs, etc., for Epstein-Barr virus, tumors, and genetics; a clinical examination database including nasopharyngoscopy, imaging, pathology, and other examinations; and databases of Epstein-Barr virus and human genetic sequencing, etc.

Eligibility

Sex
ALL
Min age
30 Years
Max age
69 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Residents with a definite native place; * Aged 30 and 69 years at screening; * Capable of long-term cooperation with screening and follow-up. Exclusion Criteria: * Known severe cardiovascular, liver or kidney disease, or neuropsychiatric disorders; * History of previous malignant tumors; * Severe autoimmune diseases or immunodeficiency; * Females with a positive pregnancy test at screening; * Inability to cooperate with the study due to psychological, social, family, and geographical reasons.

Primary outcome measure(s)

  • A data platform for an NPC screening cohort — At screening, 3 years and 10 years thereafter
    A data platform, including an NPC epidemiological information database based on the gender, age, ethnicity, dietary and lifestyle habits, and geographical environmental factors, a biobank based on various samples and screening test results, and a clinical examination database based on nasopharyngoscopy, head and neck MRI, and a database for EB virus and human genetic sequencing information.

Trial sites (1)

FacilityCityRegionStatus
The Fifth Affiliated Hospital of Sun Yat-sen University Zhuhai Guangdong Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06787456 on ClinicalTrials.gov ↗ ← All trials in China