Last reviewed · How we verify
NCT06842238: BRONCHAD
Descriptive Study of the Initial Management of Young Children With Moderate Acute BRONCHiotitis With Home Hospitalisation
trial in Bronchiolitis in 40 participants. Currently enrolling.
1 November 2025
Quick facts
| Lead sponsor | Elsan |
|---|---|
| Status | Recruiting now |
| Study type | OBSERVATIONAL |
| Enrollment | 40 |
| Start date | 1 November 2024 |
| Primary completion | 1 November 2025 |
| Estimated completion | 1 August 2026 |
| Sites | 1 location across France |
Conditions studied
- Bronchiolitis — all drugs for Bronchiolitis →
- Bronchiolitis Acute — all drugs for Bronchiolitis Acute →
Sponsor
Elsan — full company profile →
Who can join
Adults 2 Months to 2, any sex, with Bronchiolitis or Bronchiolitis Acute. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The occurrence of a first episode of acute bronchiolitis in an infant or young child (3 months-2 years) always represents a medical event that generates stress for parents and in some cases for the primary care physician when it is necessary to decide on the child's orientation for treatment. Each year, during the winter season, this pathology affects 30% of infants under two years old (480,000 annual cases in France), generates approximately 30,000 hospitalizations and exposes to an overall mortality risk of 0.08%. According to the recommendations of the HAS (2019), moderate bronchiolitis does not require systematic hospitalization and can be managed in a Home Hospitalization (HAD) context. When the child's examination data do not find signs of severity, the SpO2 measurement is greater than 92% and the family context allows for return home, HAD management is a reasonable option and represents an alternative to the classic scheme of assessing the level of severity by the emergency department and subsequent hospitalization if necessary. HAD management is carried out within the framework of a very structured "patient pathway", codified and supervised by the pediatric teams and doctors of this department. This patient pathway concerns children with a moderate form of bronchiolitis without oxygen requirements at the time of inclusion. This must be 48 hours from the onset of the child's respiratory clinical signs. The main objective of this study is to describe the need for oxygen therapy for a young child with moderate acute bronchiolitis syndrome during home hospitalization (HAD) care.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT06842238
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Bronchiolitis
Currently open trials in the same condition.
- NCT07251972 — Comparison of Two Methods of Immunoprophylaxis Against RSV in Term Newborns · active not recruiting
- NCT06862895 — Effect of Chest Physiotherapy on Clinical Outcome of Infants With Bronchiolitis · NA · recruiting
- NCT06425107 — Point-of-Care Lung Ultrasound for Prognosis in Critically Ill Infants With Acute Lower Respiratory Tract Infection · recruiting
- NCT06108648 — Efficacy of Lavender Essential Oil Chest Wraps in Infants With Bronchiolitis · Phase 4 · recruiting
- NCT06946264 — Characterization of Bronchodilator Response in Children With Bronchiolitis Using Phenotypic and Genotypic Features · Phase 3 · recruiting
Other Elsan trials
Trials by the same sponsor.
- NCT07464665 — Comparing Dual-mobility Cups Versus Unipolar Cups for Unselected Primary Total Hip Arthroplasty by Direct Anterior Appro · NA · not yet recruiting
- NCT07267572 — Evaluation of the Added Value of Logotherapy in the Psychological Support of Patients With Primary Breast Cancer · NA · not yet recruiting
- NCT07248124 — Pilot Study, Aimed at Describing in Myography, the Collapse of the Muscular Response Visualized in the Scratch Collapse · NA · recruiting
- NCT06835790 — Comparative 3-year Study of Nissen-sleeve vs. Sleeve Plus Cruroplasty in Obese Patients With Hiatal Hernia · NA · not yet recruiting
- NCT06822452 — Prospective Comparative Study Evaluating the Early Complications of Robot-assisted Radical Prostatectomy Performed as an · NA · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06842238 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Elsan
- Last refreshed: 24 February 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06842238.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing