Clinical trial Recruiting at 1 site Observational Ages 0 Months to 24 Months

RSV in young children in Ho Chi Minh City: how common and how much burden

Official title: Assessing the Epidemiological Characteristics and Clinical Burden of Respiratory Syncytial Virus (RSV) Infection in Children Aged 0-24 Months in Primary Healthcare Settings of Ho Chi Minh City, Vietnam (2026 - 2028)

Run by Tam Anh Research Institute · NCT07640581 · Data updated 2026-11-12

This study tests how often RSV occurs among children 0–24 months with ARI in three Ho Chi Minh City centers over two RSV seasons, using noninterventional observation.

More Acute Respiratory Infections (ARIs) trials

Quick facts

Study typeObservational
Ages0 Months to 24 Months
SexAll
Enrollment2000 (estimated)
SponsorTam Anh Research Institute
Academic / other
Locations3 sites (Ho Chi Minh City, Ho Chi Minh and 2 other locations)
StatusRecruiting
StartedJune 4, 2026
Main results expectedJune 4, 2028
Study endsAugust 1, 2028
Registry record updatedJune 10, 2026
Trial IDNCT07640581 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Children aged 0 to 24 months with ARI symptoms presenting at the participating sites and whose parent or legal guardian provides consent.

Probably not a fit

Children whose ARI is not due to RSV and those who do not consent may not benefit directly from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a prospective, multicenter, observational study enrolling children aged 0 to 24 months who present with acute respiratory infection symptoms. It uses continuous, convenience sampling across two epidemiological seasons (2026 and 2027) to capture RSV prevalence via nasopharyngeal swabs, alongside routine care. No change to standard treatment is made; data reflect real-world practice. The study aims to describe the epidemiology and clinical burden of RSV in this population in Vietnam's outpatient and inpatient settings. Enrollment continues until the target of 2,000 participants is reached across three sites over two seasons.

Why it matters

Potential benefit: If successful, findings could better inform clinical awareness and public health planning for RSV management in young children.

How similar studies have gone: Prior observational work in similar pediatric populations has helped describe RSV burden, though this particular two-season, multi-site design provides contextual data for Vietnam.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Children aged 0 to \<24 months (i.e., less than two years old).
* Children presenting with a diagnosis of acute respiratory infection (ARI), defined as an illness with one or more of the following symptoms: cough, rhinorrhea, sore throat, dyspnea (including wheezing, tachypnea, or apnea/increased work of breathing), sepsis (for infants aged \<6 months), and/or fever.
* Children residing in the lowest administrative division (Phường / Xã) in Vietnam that is designated for the specific study site (outpatient clinic or community hospital). As patients live in the same administrative district as the healthcare facility, this will facilitate follow-up and ensure that the study results are representative of the range of severity of ARI presenting to each specific study site.
* Parent or LAR provides written informed consent for their child's participation.

Exclusion Criteria:

* Children whose mothers received a maternal RSV vaccine during pregnancy or who have themselves received RSV-specific monoclonal antibodies (mAbs).
* Children with a known non-respiratory cause for hospitalization.
* Children with respiratory symptoms lasting over 14 days.
* Children hospitalized elsewhere within the preceding 4 days, excluding admission to the Emergency Department.
* Children already enrolled in another RSV study within the preceding 3 months.

Where it's running

  • Di An Medical Center
    Ho Chi Minh City, Ho Chi Minh, Vietnam
    Recruiting
  • Ba Ria General Hospital
    Ho Chi Minh City, Ho Chi Minh, Vietnam
    Not yet recruiting
  • Le Van Thinh Hospital
    Ho Chi Minh City, Ho Chi Minh, Vietnam
    Not yet recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.