RSV ComNet III: Disease Burden of RSV

Sponsor
Hospices Civils de Lyon (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05506670
Collaborator
(none)
300
1
7
43.1

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Diagnostic test and phone call
  • Diagnostic Test: Diagnostic test

Study Design

Study Type:
Observational
Anticipated Enrollment :
300 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Disease Burden of RSV in Young Children in Primary Care
Anticipated Study Start Date :
Oct 1, 2022
Anticipated Primary Completion Date :
May 1, 2023
Anticipated Study Completion Date :
May 1, 2023

Arms and Interventions

Arm Intervention/Treatment
proved RSV infection (RSV positive patients

Other: Diagnostic test and phone call
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.

suspected but not proved RSV infection (RSV negative patients)

Other: Diagnostic test and phone call
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.

Outcome Measures

Primary Outcome Measures

  1. Clinical burden of RSV acute respiratory infections [Day 14]

    Persistent symptomatology at D14

  2. Clinical burden of RSV acute respiratory infections [Day 30]

    Persistent symptomatology at D30

Eligibility Criteria

Criteria

Ages Eligible for Study:
0 Years to 5 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Centre d'Investigation Clinique de Lyon- Groupement Hospitalier Est- Hospices Civils de Lyon Bron Rhone France 69500

Sponsors and Collaborators

  • Hospices Civils de Lyon

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hospices Civils de Lyon
ClinicalTrials.gov Identifier:
NCT05506670
Other Study ID Numbers:
  • 69HCL22_0703
First Posted:
Aug 18, 2022
Last Update Posted:
Aug 18, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Hospices Civils de Lyon
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 18, 2022