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Recruiting Observational

Surveillance and Tracking the Outcomes of Chronic Latent EBV Infection

NCT03491605 · tracked via the Priya Life Science China tracker
Phase
Observational
Started
2019-07-01
Last updated
2021-02-10

Condition(s) studied

EBV Infection

Investigational drug(s) / intervention(s)

peripheral EBV-DNA load

peripheral EBV-DNA load: No intervention

Study summary

Immunocompetent subjects with high load of Epstein-Barr virus DNA (EBV-DNA) in peripheral blood will be enrolled and prospectively followed up to track the natural histories of the chronic high load of EBV virus. The primary goal of this study is to explore the association of peripheral high load of EBV with the hematological malignancies, and second goal is to investigate the genetic mechanisms of immune escape and tumorigenesis of chronic EBV infection.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. immunocompetent subjects who was found to have high EBV-DNA load (\>1×103 copies/ml)in peripheral blood during the physical examination 2. Willing to be followed up by telephone or face-to-face interview Exclusion Criteria: 1. Subjects with defined immunodeficiency 2. Subjects who have taken or are going to take immunosuppressive drugs. 3. Subjects Diagnosed a validated hematopathy 4. Subjects diagnosis as precancerous lesion or malignant tumor and the life expectancy is less than 1 year. 5. psychological illness which does not allow subjects to understand the study and participate following his own free will 6. Pregnant woman 7. no written informed consent

Primary outcome measure(s)

  • hematological malignancies — Five years or more if necessary
    including Burkitt lymphoma, EBV+ B-cell lymphoproliferative diseases, extranodal NK/T-cell lymphoma of nasal type (ENKL), aggressive NK-cell leukemia (ANKL), classic Hodgkin lymphoma, and Chronic active Epstein-Barr virus infection (CAEBV).

Trial sites (1)

FacilityCityRegionStatus
Tongji hospital, Tongji medical collage of HUST Wuhan Hubei 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 NCT03491605 on ClinicalTrials.gov ↗ ← All trials in China