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A randomized controlled study of antiviral therapy in children with infectious mononucleosis

A randomized controlled study of antiviral therapy in children with infectious mononucleosis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043741
Enrollment
Unknown
Registered
2021-02-27
Start date
2021-02-15
Completion date
Unknown
Last updated
2021-06-28

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

Conditions

Infectious mononucleosis

Interventions

Acyclovir treatment group:Acyclovir antiviral treatment, and general symptomatic treatment
Ganciclovir treatment group:Ganciclovir antiviral treatment, and general symptomatic treatment
Blank control group:Rehydration, heart protection, liver protection and other symptomatic treatment

Sponsors

Beijing Children's Hospital Affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients with onset age of 1-18 years old; 2. Patients who meet the diagnostic criteria of infectious mononucleosis in the "recommendations on the principles of diagnosis and treatment of major non neoplastic Epstein Barr virus infection related diseases in children" formulated by the infectious diseases group of Chinese Medical Association and the National Children's Epstein Barr virus infection cooperation group in 2016; 3. Patients with persistent fever (T > 37.5 degrees C) and fever <= 5 days before hospitalization.

Exclusion criteria

Exclusion criteria: 1. Patients allergic to acyclovir and ganciclovir; 2. Patients with severe primary cardiovascular diseases, kidney diseases, liver diseases, respiratory diseases, hematological diseases, malignant tumors, endocrine and metabolic diseases, primary immunodeficiency diseases, or serious diseases affecting their survival; 3. Patients with high probability of bacterial infection according to symptoms, signs or laboratory examination; 4. Patients with steroid hormone or other immunosuppressant use history within 2 weeks before enrollment; 5. Patients with history of antiviral treatment within 2 weeks before enrollment; 6. Children with different opinions.

Design outcomes

Primary

MeasureTime frame
Duration of fever;

Secondary

MeasureTime frame
Liver dysfunction;Other organs dysfunction;

Countries

China

Contacts

Public ContactHuili Hu

Beijing Children's Hospital Affiliated to Capital Medical University

18701466081@163.com+86 18701466081

Outcome results

None listed

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