Condition: Acute Respiratory Infections (ARIs) · Sponsor: Tam Anh Research Institute
This is a prospective, observational, multicenter study employing continuous, convenience sampling, stratified by study site and by fortnightly interval, enrolling until the target sample sizes are achieved over the first epidemiological season (2026) and the second epidemiological season (2027). The study population includes children aged 0 to 24 months presenting to the outpatient or inpatient facilities of the study sites with signs and symptoms of acute respiratory infection (ARI). In Vietnam there is no single guideline for diagnosing ARI, but rather there are guidelines specific to clinical conditions such as pharyngitis, rhinitis, tonsilitis, or pneumonia. This study will use an operational definition where ARI is defined as the presence of one or more of the following clinical features: cough, rhinorrhea, sore throat, dyspnea, and / or fever. RSV testing using nasopharyngeal (NP) swabs will be collected from all eligible children with consent to participate in the study; if a NP swab is not feasible, a mid-turbinate nasal swab will be used. Specimens will be transported to a central laboratory for real-time, reverse transcription-polymerase chain reaction (RT-PCR) testing. Furthermore, the stored viral transport media from all the RSV-positive samples will be used for whole genome sequencing (WGS) to determine the subgroup (A or B) of the circulating RSV strains and to analyze the genotype. The parent or legally acceptable representative (LAR) of pediatric patients…
This description comes directly from the study's public registry record.
Dung Van Do, MD, PhD · 84918382253. · dungdv@tamri.vn
Always discuss trial participation with your own doctor first.
| Ba Ria General Hospital | Ho Chi Minh City, Ho Chi Minh, Vietnam | Not Yet Recruiting |
| Di An Medical Center | Ho Chi Minh City, Ho Chi Minh, Vietnam | Recruiting |
| Le Van Thinh Hospital | Ho Chi Minh City, Ho Chi Minh, Vietnam | Not Yet Recruiting |
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Source record: clinicaltrials.gov/study/NCT07640581