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Efficacy Evaluation of Tocilizumab in the treatment of severe fever with thrombocytopenia syndrome

Efficacy Evaluation of Tocilizumab in the treatment of severe fever with thrombocytopenia syndrome

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076317
Enrollment
Unknown
Registered
2023-10-01
Start date
2023-10-01
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Severe fever with thrombocytopenia syndrome

Interventions

Intervention:Symptomatic treatment+Tocilizumab

Sponsors

The Eighth Medical Center of Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients diagnosed with SFTS through laboratory testing

Exclusion criteria

Exclusion criteria: ? Age<18 years old; ? The patient has received systematic antiviral therapy or immunotherapy within 6 months. ? Patients have severe progressive chronic diseases or tumors, such as severe heart failure, severe liver and kidney failure, and other important organ failure, as well as hematological tumor diseases or uncontrolled solid tumors; ? Patients with poor immune function or active tuberculosis infection; ? Patients who are allergic to Tocilizumab; ? PLT < 20 × 10^9/L; ? Pregnant and lactating women; ? Subject is unwilling or unable to follow protocol procedures

Design outcomes

Primary

MeasureTime frame
Case fatality rate of SFTS;

Secondary

MeasureTime frame
Days required for PLT and WBC to return to normal levels;Time to resolution of main clinical symptoms and viral load;Time for blood biochemical indicators to return to normal levels;IL-6 serum level;adverse event;

Countries

China

Contacts

Public ContactBao Pengtao

The Eighth Medical Center of Chinese PLA General Hospital

bao03@163.com+86 159 1061 4585

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 8, 2026