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NCT05582239: RESPIVAC

Measure of Vaccine Effectiveness to Prevent Hospitalizations for Viral Respiratory Infections in Adults

Status unknown Last updated 17 May 2023
What this trial tests

trial in Severe Acute Respiratory Infection (SARI) in 2,400 participants. Status unknown.

Timeline
20 January 2023
Primary endpoint
20 January 2026
20 January 2026

Quick facts

Lead sponsorANRS, Emerging Infectious Diseases
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment2,400
Start date20 January 2023
Primary completion20 January 2026
Estimated completion20 January 2026
Sites8 locations across France

Conditions studied

Sponsor

ANRS, Emerging Infectious Diseases — full company profile →

Who can join

18 and older, any sex, with Severe Acute Respiratory Infection (SARI) or Influenza. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is a prospective, multicentric, observational test negative design study on adults hospitalized for Severe Acute Respiratory Infection (SARI), regardless of their vaccination status.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. SARS-CoV-2 versus Influenza A Virus: Characteristics and Co-Treatments.
    Wang X, Li J, Liu H, Hu X, et al · · 2023 · cited 7× · PMID 36985154 · DOI 10.3390/microorganisms11030580

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Other ANRS, Emerging Infectious Diseases 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/NCT05582239.

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