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The efficacy of peramivir in children with different subtypes of influenza and related influencing factors

The efficacy of peramivir in children with different subtypes of influenza and related influencing factors

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200056590
Enrollment
Unknown
Registered
2022-02-08
Start date
2022-02-07
Completion date
Unknown
Last updated
2024-10-21

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

Conditions

Influenza

Interventions

Group Influenza A H1N1:Intravenous peramivir
Group Influenza A H3N2:Intravenous peramivir
Group Influenza B Victoria:Intravenous peramivir

Sponsors

Suqian Hospital of Nanjing Drum Tower Hospital Group
Lead Sponsor

Eligibility

Sex/Gender
All
Age
28 Days to 18 Years

Inclusion criteria

Inclusion criteria: 1. The throat swab of the patient was tested by RT-PCR influenza virus nucleic acid detection kit, and the result was positive for influenza. 2. The children should be over 28 days old and under 18 years old (this project does not include newborns under 28 days old).

Exclusion criteria

Exclusion criteria: 1. Allergic to NA inhibitors; 2. Those who have used antiviral drugs (such as amantadine, rimantadine, oseltamivir, zanamivir, nucleosides, etc.) in the past 1 month; 3. Patients with basic diseases (such as liver and kidney insufficiency, heart insufficiency, nervous system diseases, etc.).

Design outcomes

Secondary

MeasureTime frame
Time to fever alleviation;Cough to fever alleviation;

Primary

MeasureTime frame
The duration of virus nucleic acid positivity;The remission time of clinical symptoms;

Countries

China

Contacts

Public ContactChen Hongdou

Suqian Hospital of Nanjing Drum Tower Hospital Group

chenhongdou2000@aliyun.com+86 13365252813

Outcome results

None listed

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