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NCT Number: NCT04515446

Quantification of Viral Load in the Upper Respiratory Tract in Patients Treated With Olsetamivir for Influenza

Seasonal influenza is a frequent disorder with high impact on morbidity and mortality and significant burden on healthcare-related cost. In France, the 2018-2019 flu epidemic has led to 13,100 all-cause death including 9,900 death directly related to the viral infection.

As cross-transmission of influenza is responsible for nosocomial outbreaks, preventing transmission of infectious agents in healthcare settings is a major issue. If vaccination of patients and healthcare givers remains cornerstone, control procedures are mandatory. Therefore patients admitted with influenza require isolation precautions including admission in a single room and protective measures. Based on experts advise, isolation is currently recommended for 5 to 8 days. Duration of isolation depends on immune status and antiviral therapy. However, during periods of epidemic, every hospital room is valuable and each ressource has to be tightly used. Risk of contamination is related to the presence of influenza in the upper airways. To the Promoteur 's knowledge, presence of influenza in the upper airways has not been studied in patients receiving oseltamivir. The question is : Do duration of isolation in patients admitted with flu decreas when they are treated with antiviral therapy. To answer this question The Promoteur would aim to determine influenza carriage in the upper airways in in-patients treated by olsetamivir.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Centre Hospitalier Princesse Grace

Monaco, Municipality of Monaco, 98000

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patients (≥18 years)
  • Positive testing for influenza (A or B)
  • Patients hospitalized and treated with olsetamivir
  • Signature of informed consent
  • Affiliation to healthcare insurance (France, Monaco)

Exclusion criteria

  • Refusal to participate
  • Admission to intensive care
  • Palliative care
  • Unable to give inform consent
  • Patients under legal protection

Treatment and study plan

Rapid test for diagnosis orientation

Diagnostic Test

Rapid tests screen for influenza viruses in less than 30 minutes. They detect internal viral nucleoproteins by immunochromatography using specific antibodies attached to one or more strips.

Other names: TROD

Quantitative PCR

Diagnostic Test

Molecular biology method of gene amplification in vitro. It allows a large number of known DNA or RNA sequences to be duplicated

Primary outcomes

  1. The duration of influenza virus carriage in the upper airways in patients treated with olsetamivir will be observed

    Time frame: Within 8 days following patient's participation

Secondary outcomes

  1. Duration of influenza virus carriage in the upper airways among patients treated with olsetamivir according to the viral strand (A or B) will be mesured

    Time frame: Within 8 days following patient's participation

  2. Duration of influenza virus carriage in the upper airways among patients treated with olsetamivir according to their vaccination status and comorbidities will be mesured and compared

    Time frame: Within 8 days following patient's participation

  3. Difference in the number of days in isolation in patients hospitalized and treated with olsetamivir will be evaluated

    Time frame: 21 months

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire de Nice

Other

Collaborators

  • Centre Hospitalier Princesse Grace

Registry information

Official study title

Sequential Quantification of Viral Load in the Upper Respiratory Tract in Adult Patients Admitted for Influenza and Treated With Olsetamivir

Acronym: VIRIDAE

Important dates

Study start
2020
Primary completion
2023
Study completion
2026
First posted
Aug 17, 2020
Registry last updated
Dec 8, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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