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Completed

NCT Number: NCT05506670

Disease Burden of RSV

Respiratory diseases are one of the leading causes of morbidity and mortality among young children, and respiratory syncytial virus (RSV) is the most common pathogen causing these respiratory diseases in this age group. RSV can present in the form of a variety of clinical syndromes, including upper respiratory tract infections, bronchiolitis, pneumonia, exacerbations of asthma and viral-induced wheeze. RSV is highly seasonal and occurs mostly during winter seasons in temperate climates. Sixty to seventy percent of all children experience an RSV infection before the age of one, and nearly all do so before the age of two.(

'Burden of disease' is a general term without a universally accepted definition and refers to the human and economic costs that result from poor health. RSV 'burden of disease' studies in young children (aged 0-4 years), have mostly been focused on the morbidity and mortality rates of RSV infections. The socio-economic burden of RSV infections in young children has been studied, however, a meta-analysis showed that of the 365,828 RSV disease episodes included in cost-analysis studies, only 27,286 (7.4%) focused on outpatient and emergency cases. To our knowledge, only two outpatient studies have prospectively investigated the clinical and socio-economic burden of laboratory confirmed RSV infections in young children; and both studies collected data in the early 2000s. More recently, one study has investigated the health care use, duration of illness and complications associated with RSV in a cohort of newborn infants. There is therefore a lack of knowledge on the clinical and socio-economic disease burden of RSV infections in young children in primary care.

Current treatment options for RSV infections are limited to supportive care. The only available antiviral monoclonal antibody (mAb) 'Palivizumab' is considered cost-effective for certain high-risk group infants and requires monthly injections during winter. New candidate RSV vaccines and mAbs (with longer half-life times) are in late-stage clinical trials. Therefore, accurate estimates of the burden of RSV infections, including in primary care, are crucial to better assess the overall impact RSV infections may have on the society.

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Key information

Age range

0 year–5 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Centre d'Investigation Clinique de Lyon- Groupement Hospitalier Est- Hospices Civils de Lyon, Bron, Rhone, France

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Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age <5 years
  • Consulting a primary care practitioner with symptoms of an acute respiratory infection (ARI)
  • Participation agreement of at least one of the two parents/legal guardians before intervention

Follow-up criterion

  • Sampled children with a lab-confirmed diagnosis of RSV.

Exclusion criteria

  • Signs of severity (moderate to severe respiratory distress, oxygen saturation SpO2 < 92%, dehydration, Glasgow < 13) for children < 3 month-old in emergency department
  • No consultation with a doctor in the previous 24 hours
  • Insufficient knowledge about the national language by the parents/legal guardians
  • Intellectual disabilities of the parents/legal guardians
  • Special personal circumstances in the family (based on the judgement of the primary care physician e.g. a recent death in the family)

Treatment and study plan

Diagnostic test and phone call

Other

Viral diagnostic test will be performed at inclusion. In case of RSV positive results, follow up phone calls will be scheduled at day 14 and day 30 to collect data.

Diagnostic Test

Diagnostic Test

Viral diagnostic test will be performed at inclusion. In case of RSV negative result, no more intervention will be required.

Primary outcomes

  1. Clinical burden of RSV acute respiratory infections

    Time frame: Day 14

    Persistent symptomatology at D14

  2. Clinical burden of RSV acute respiratory infections

    Time frame: Day 30

    Persistent symptomatology at D30

Sponsors and collaborators

Lead sponsor

Hospices Civils de Lyon

Other

Registry information

Official study title

Disease Burden of RSV in Young Children in Primary Care

Acronym: RSV ComNet III

Important dates

Study start
2022
Primary completion
2024
Study completion
2024
First posted
Aug 18, 2022
Registry last updated
Jul 8, 2024

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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