A Prospective Study on the Application of Saliva EBV-DNA Detection in EBV Infection Related Diseases
Trial Snapshot
- Phase
- Not Applicable
- Sponsor
- Beijing Friendship Hospital
- Enrollment
- 40
- Locations
- 1
- Primary Endpoint
- Monitoring
Study Overview
Brief Summary
This study is a single-center, prospective, observational clinical study to evaluate the Application of saliva EBV-DNA Detection in EBV Infection Related Diseases
Study Design
- Study Type
- Observational
- Observational Model
- Case Only
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 3 Years to 65 Years (Child, Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •According to the HLH-04 diagnostic criteria, it meets the HLH diagnostic criteria. EBV infection occurs in cells with EBV-DNA copy number significantly increased in peripheral blood or tissue, or where EBV coding small RNA(EBER) is detected in tissue or peripheral blood. Or Straus' 1988 diagnostic criteria for CAEBV.
- •Informed consent
Exclusion Criteria
- •Patients who cannot cooperate with saliva collection
- •Patients who are unwilling to cooperate with the project research according to the project research plan.
Outcomes
Primary Outcomes
Monitoring
Time Frame: 2 to 12 weeks after treatment
The sensitivity and specificity of saliva EBV-DNA detection level as a monitoring method for EBV infection-related diseases, and whether it can replace peripheral blood EBV-DNA monitoring
Diagnosis
Time Frame: baseline
The sensitivity and specificity of saliva EBV-DNA detection level as a diagnosis for EBV infection-related diseases, and whether it can replace peripheral blood EBV-DNA monitoring
Secondary Outcomes
No secondary outcomes reported
Investigators
Zhao Wang
Principal Investigator
Beijing Friendship Hospital
