Skip to content

Comparison of Effectiveness in Reducing Severity of Illness in Influenza Pediatric Outpatients Treated With BXM or Neuraminidase Inhibitors - 2018/19, 2019/20 influenza season data -

Comparison of Effectiveness in Reducing Severity of Illness in Influenza Pediatric Outpatients Treated With BXM or Neuraminidase Inhibitors - 2018/19, 2019/20 influenza season data - - Comparison of Effectiveness in Reducing Severity of Illness in Influenza Pediatric Outpatients Treated With BXM or Neuraminidase Inhibitors - 2018/19, 2019/20 influenza season data -

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000051678
Enrollment
200000
Registered
2023-07-24
Start date
2023-07-18
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

None listed

Sponsors

Shionogi & Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1, Patients whose the date of earliest diagnosis of influenza virus infection is within each influenza season (day 1) during the enrollment period of each influenza season (October 1, 2018 to April 17, 2019, or October 1, 2019 to April 17, 2020) and patients has an observable period from 6 months before Day 1 (that is, the observation start date in the parameter table is more than 6 months before the month of Day 1). Influenza virus infection is defined by the ICD-10 small classification code without a suspicion flag. 2, Patients with BXM, OTV, ZNV, or LNV administration date as anti-influenza virus drugs on Day 1.

Exclusion criteria

Exclusion criteria: 1, Patients with an admission receipt or DPC receipt with the date of admission from 90 days before Day 1 2, Patients who have administration dates of an antibacterial drugs from 90 days prior to Day 1 3, Patients who has a diagnosis (no suspicion flag) of pneumonia in receipts for the past 3 months from the month with Day 1 to excluding the month with Day 1, or has a medical starting date before Day 1 to including Day 1 in receipts for the month including Day 1. 4, Patients who have infusions on Day 1 5, Patients with febrile seizures on Day 1 with medical starting date (no suspicion flag) 6, Patients who died on Day 1 (Patients for whom "terminate in death" is described in the disease name in the receipt for the month including Day 1 and whose last date of medical treatment in the receipt is the same as Day 1). 7, Patients under 5 years old or 12 years old or older as of Day 1 8, Patients with multiple influenza anti-influenza drugs (BXM, OTV, ZNV, LNV, or PRV) dispensing dates on Day 1.

Design outcomes

Primary

MeasureTime frame
Hospitalization incidence (days 2-14) with the date of diagnosis of influenza infection as Day 1

Secondary

MeasureTime frame
Incidence of each of the following events from Day 2 to Day 14 - Antibacterial oral administration - Antibacterial injectable administration - Pneumonia - Additional anti-influenza drug use - Infusion - Febrile seizures - Each secondary end points with hospitalization

Countries

Japan

Contacts

Public ContactShogo Miyazawa

Shionogi & Co., Ltd. Data Science Department

shogo.miyazawa@shionogi.co.jp+819030566073

Outcome results

None listed

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