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NCT07164430

The Impact of the 2025 Infant and Maternal Respiratory Syncytial Virus (RSV) Prevention Program on RSV-related Hospitalisations in the Australian Capital Territory

Completed Last updated 5 March 2026
What this trial tests

trial in Respiratory Syncytial Virus (RSV) Infection in 2,792 participants. Completed in 31 January 2026.

Timeline
22 September 2025
Primary endpoint
31 January 2026
31 January 2026

Quick facts

Lead sponsorNicola Irwin
StatusCompleted
Study typeOBSERVATIONAL
Enrollment2,792
Start date22 September 2025
Primary completion31 January 2026
Estimated completion31 January 2026
Sites1 location across Australia

Conditions studied

Sponsor

Nicola Irwin

Who can join

Under 2, any sex, with Respiratory Syncytial Virus (RSV) Infection or Respiratory Syncytial Virus Hospitalizations. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this observational study is to is to examine the impact of new RSV prevention medicines on the burden of RSV disease among young children. The main question it aims to answer is: What was the impact of the 2025 RSV prevention program on RSV-related hospitalisation in children under 2 years of age? Participants won't need to do anything additional for the study as only routinely collected health information will be used to answer the research question.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Nicola Irwin trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07164430.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing