Viral Respiratory Tract Infections

2

Review clinical trials related to Viral Respiratory Tract Infections. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

PremaBiom: Metatranscriptomics of the Respiratory Microbiome to Predict the Occurrence of Bronchopulmonary Dysplasia in Preterm Infants

The goal of this clinical trial is to understand the impact of respiratory microbiome maturation in respiratory health of preterm infants under 32 gestational weeks. The main questions it aims to answer are: * What is the role of microbiome maturation in respiratory health (development of bronchopulmonary dysplasia, childhood asthma and viral respiratory infections) of preterm infants ? * Which environmental or health factors are involved in the maturation of the respiratory microbiome ? Participants will undergo follow-up from birth until 3 years of corrected age including nasal swabs, stool samples, and for some of them blood and milk sample.

Participants needed: 270
Trial details
Age: Up to 72Biological sex: AllType: InterventionalSponsor: University Hospital, CaenUpdated: Feb 13, 2026Locations: 6
Eligibility criteria

Preterm infants with gestational age at birth lower than 32 gestational weeks an... [+3]

Palliative care only [+3]

Status: Recruiting

The Fever Clinic Acute Respiratory Cohort

This prospective cohort study aims to characterize the natural progression and outcomes of acute respiratory infections among patients presenting to fever clinics. At enrollment, patients' clinical symptoms, laboratory findings, and chest imaging data will be collected. Longitudinal follow-up will be conducted to evaluate disease progression, complications, and long-term outcomes. As an observational study, no interventions are involved; all patients receive routine clinical management as directed by their attending physicians. This real-world study design enables the assessment of the natural course of acute respiratory infections and the identification of factors associated with clinical outcomes.

Participants needed: 1,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Fudan UniversityUpdated: Dec 12, 2025Locations: 1Duration: 30 Days
Eligibility criteria

Age ≥ 18 years (based on official identification document). [+4]

Inability to provide independent informed consent due to impaired consciousness... [+3]