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Disease Burden of RSV (RSV ComNet III)

Civil Hospices of Lyon logo

Civil Hospices of Lyon

Status

Completed

Conditions

RSV Acute Respiratory Infection

Treatments

Other: Diagnostic test and phone call
Diagnostic Test: Diagnostic test

Study type

Interventional

Funder types

Other

Identifiers

NCT05506670
69HCL22_0703

Details and patient eligibility

About

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.

Enrollment

84 patients

Sex

All

Ages

Under 5 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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

Follow-up criterion

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

Exclusion criteria

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

Trial design

Primary purpose

Other

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

84 participants in 2 patient groups

proved RSV infection (RSV positive patients
Experimental group
Treatment:
Diagnostic Test: Diagnostic test
Other: Diagnostic test and phone call
suspected but not proved RSV infection (RSV negative patients)
Experimental group
Treatment:
Diagnostic Test: Diagnostic test
Other: Diagnostic test and phone call

Trial contacts and locations

6

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Central trial contact

Aurelie PORTEFAIX, Dr; Tiphanie GINHOUX

Data sourced from clinicaltrials.gov

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