ECOBRON: Lung Ultrasound in Bronchiolitis
Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS (Other)
Overall Status
Completed
CT.gov ID
NCT05741177
Collaborator
(none)
300
1
36
8.3
Study Details
Study Description
Brief Summary
prospective assessment of lung ultrasound score in children with different severities of bronchiolitis
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Study Design
Study Type:
Observational
Actual Enrollment
:
300 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Studio Osservazionale, Prospettico, Multicentrico, No-profit Sull' utilità Dell' ECOgrafia Pleuro-polmonare Nella Gestione Delle BRONchioliti Nella Popolazione Pediatrica di età ≤12 Mesi - ECO-BRON
Actual Study Start Date
:
Jan 1, 2019
Actual Primary Completion Date
:
Jan 1, 2021
Actual Study Completion Date
:
Jan 1, 2022
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
bronchiolitis children with bronchiolitis |
Diagnostic Test: lung ultrasound
lung ultrasound score
|
Outcome Measures
Primary Outcome Measures
- lung ultrasound score predict bronchiolitis severity [1 year]
lung ultrasound score predict bronchiolitis severity
Eligibility Criteria
Criteria
Ages Eligible for Study:
0 Months
to 12 Months
Sexes Eligible for Study:
All
Inclusion Criteria:
- children with bronchiolitis
Exclusion Criteria:
- children with bronchiolitis and comorbidities
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Gemelli Hospital | Rome | Italy | 00168 |
Sponsors and Collaborators
- Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
ClinicalTrials.gov Identifier:
NCT05741177
Other Study ID Numbers:
- ID 2021
First Posted:
Feb 23, 2023
Last Update Posted:
Feb 23, 2023
Last Verified:
Feb 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms: