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
  • Diagnostic Test: lung ultrasound

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

  1. 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:

Study Results

No Results Posted as of Feb 23, 2023