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RSV InfectionNCT07264478

Diagnosis and Treatment Status and Medical Burden of Respiratory Syncytial Virus Infection in Children in China

An observational study of RSV Infection and Disease Burden, run by Beijing Children's Hospital at 1 site in China.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record

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Trial summary

To understand the diagnosis and treatment status and medical burden of respiratory syncytial virus (RSV) infection in children in China, and to provide scientific basis for formulating prevention and treatment strategies for children. Read more about this study

Who is it for?
Ages 0 to 18 years
Conditions the study is for
RSV Infection, Disease Burden
What is being tested?
uninvolved
How many people
1,100 participants
Where
1 siteChina
Study dates
15 Oct 2022to 30 Dec 2025
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 0 to 18 years
  • All sexes
  • No healthy volunteers
  • Child, Adult

Study population: According to the seven administrative regions of China, namely Northeast, North, Northwest, Southwest, Central, South and East China, 1-3 children's medical institutions were selected from each region, and the cases of bronchiolitis or pneumonia admitted to hospitals and diagnosed as RSV positive by etiology during January 1, 2017 to December 31, 2021 were selected. A total of 11 hospitals were selected, each with 100 children, a total of 1100 cases

Who may be able to join

  • Hospitalized patients under 18 years of age with an etiological diagnosis of RSV-positive bronchiolitis or pneumonia

Who cannot join

  • Inpatients under 18 years of age with an etiological diagnosis of RSV-positive bronchiolitis or pneumonia are excluded from any of the following criteria:
  • Pneumonia occurring 48 hours after hospitalization;
  • Combined with bronchial foreign body;
  • Participants in clinical trials of drugs or medical devices;
  • Not complete personal and family history and other relevant information.

Trial locations and contacts

1 site in 1 country.

China1 site
  • Beijing Children's Hospital

    Beijing, Beijing Municipality, 100045

Other trials in China

About this study

Official title: Beijing Children's Hospital, Capital Medical University, China National Clinical Research Center of Respiratory Diseases, National Center for Children's Health, Beijing, China

To understand the diagnosis and treatment status and medical burden of respiratory syncytial virus (RSV) infection in children in China, and to provide scientific basis for formulating prevention and treatment strategies for children. According to the seven administrative regions of China, namely Northeast, North, Northwest, Southwest, Central, South and East China, 1-3 children's medical institutions were selected from each region, and the cases of bronchiolitis or pneumonia admitted to hospitals and diagnosed as RSV positive by etiology during January 1, 2017 to December 31, 2021 were selected. Demographic data and clinical information were collected, and subgroup analysis was designed to explore the relationship between them and medical expenses and clinical treatment burden.

Being tested
uninvolved
Medical subject headings
Respiratory Syncytial Virus Infections

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • uninvolvedOther

    uninvolved

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. hospitalization costs

    hospitalization costs,pharmcost,testcost,testcost

    Measured: duration of hospital stay

Secondary outcomes (1)
  1. hospital day

    duration of hospital stay

    Measured: duration of hospital stay

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Dec 2025
  2. Study start15 Oct 2022
  3. Primary completion12 Dec 2025 (estimated)
  4. Study completion30 Dec 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
1,100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07264478
Sponsor's protocol ID
BCH lung 22
Status last verified
Dec 2025
First submitted
12 Oct 2023
Last updated
4 Dec 2025
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

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