NCT07232550Recruiting
Biomarkers and Respiratory Omics as New CHildren Opportunities - Study of Clinical Outcomes and Predictivity Evaluation
Biomarkers and Respiratory Omics as New CHildren Opportunities - Study of Clinical Outcomes and Predictivity Evaluation - a Multi-cohort, Multi-center Study
Source: ClinicalTrials.gov · Last updated 30 Jul 2026
Brief summary (registry, in English)
The goal of this observational study is to improve the identification of biomarkers that predict disease progression and to assess the effectiveness of current therapies in children with asthma and protracted bacterial bronchitis. The main aim of the study is to evaluate the microbiome composition and diversity, cellular composition, and metabolomic profile. In addition, to assess their correlation on subsequent treatment and disease course in children with asthma, protracted bacterial bronchitis, and in those receiving inhaled glucocorticosteroids without a diagnosis of asthma. Participants will undergo fiberoptic bronchoscopy. During bronchoscopy, the performing physician will collect Bronchoalveolar lavage fluid samples for metagenomic and metabolomic analysis, as well as mucosal biopsies for histopathological evaluation.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 160 (estimated)
- First submitted
- 25 Sept 2025
- Start date
- 6 Mar 2026
- Primary completion date
- Dec 2035
- Lead sponsor
- Medical University of Warsaw
- Diseases
- Asthma
- NCT number
- NCT07232550
What you commit to
- Study type: Observational
- Planned participants: 160
- From 6 Mar 2026 to the primary completion date, Dec 2035
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Active acute respiratory infection up to 4 weeks before the procedure
- Taking antibiotics or systemic glucocorticosteroids up to 4 weeks before the procedure
Other illness
- Patients with very severe comorbidities (congenital immunodeficiencies, genetic disorders, neurological or neuromuscular diseases, cancer, severe congenital heart defects, heart failure, liver failure, inflammatory bowel disease, celiac disease)
- Patients with blood clotting disorders
- Children with diagnosed respiratory diseases other than asthma and protracted bacterial bronchitis - including interstitial diseases, tuberculosis, inflammation of small and medium-sized blood vessels
Other
- Patients for whom \>48 hours have passed between suspicion of foreign body aspiration and interventional bronchoscopy
- Children with foreign body aspiration having a foreign body located in the trachea
Who the study is looking for
- Age at the beginning of the study 0-17 years old
- Clinical indication and qualification by the attending physician for fiberoptic bronchoscopy under general anesthesia:
- Obstruction of the airways:
- Suspicion of foreign body aspiration
- Persistent stridor
- Abnormal result of functional tests of respiratory system - flattening of inspiratory or expiratory curve, presence of restriction (tested vital capacity \<5 percentile) or irreversible obstruction (persistence of Tiffneau index \<5 percentile despite administration of bronchodilators)
- Radiological findings located in the course of the larynx, trachea or bronchi
- Persistent atelectasis on subsequent radiological examinations
- Persistent cough \>4 weeks
- Hemoptysis
- Suspected laryngomalacia or tracheobronchomalacia
- Suspected tracheoesophageal fistula
- Persistent dyspnea unresponsive to anti-asthmatic treatment used for min. 2 months, with no other identifiable causes
- Radiologically detected mediastinal abnormalities
- Suspected presence of a vascular ring
- Presence of excessive secretions that are impossible for the patient to expectorate
- Fine needle biopsy of cystic lesions
- Obtained consent from patient/legal guardian for participation in the study
Age in the registry: - to 17 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Żwirki i Wigury 63A Coordinator of this site? Confirm its status | Warsaw | Poland | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.