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A multicenter, randomized controlled study of the clinical efficacy of intravenous peramivir versus oseltamivir against influenza A and B virus infection in high-risk patients

A multicenter, randomized controlled study of the clinical efficacy of intravenous peramivir versus oseltamivir against influenza A and B virus infection in high-risk patients - Comparative study of peramivir and oseltamivir in the influenza virus infection

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000009479
Enrollment
120
Registered
2012-12-05
Start date
2012-11-27
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Influenza virus infection

Interventions

Peramivir, Intravenously administration 600mg once a day, allowing daily injection if the patient condition is severe. Oseltamivir, Orally administration, 75mg twice a day for 5 days.

Sponsors

Nagasaki evaluation organization for clinical interventions
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The patients who satisfied below 1)-7): 1)Age:>=20 2)Agreement with documents 3)Fever>=38.0 degrees centigrade 4)>=2 items of ISS* which as moderate symptoms 5)Within 48hour after onset: Onset time is defined as below (1)First time at increase of body temperature (>=1 degrees centigrade as usual) (2)First time which the patient aware >=1 items of ISS* 6)Positive for Rapid Antigen Test kit 7)With at least one risk factor *ISS=Influenza Symptoms Severity

Exclusion criteria

Exclusion criteria: 1)contraindication of peramivir and oseltamivir 2)pregnant or probable pregnant women 3)Inappropriate judged by doctors 4)pneumonia on the 1st day of visiting hospital

Design outcomes

Primary

MeasureTime frame
The duration of fever

Secondary

MeasureTime frame
Symptoms of influenza infection, viral titer and subtype, complications, exacerbation of underlying diseases, H275Y mutation of the virus isolated from the patients with poor clinical effects, The detection of colonized pneumococcus in nasal pharynx in the patients complicated secondary bacterial pneumonia

Countries

Japan

Contacts

Public ContactTaiga Miyazaki

Nagasaki evaluation organization for clinical interventions office

shinkin@peath.co.jp095-819-7273

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026