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The ECOVITA Study - Validation of LUS Score in SARS-CoV-2 Disease, i.e COVID-19

ECOVITA Study. Observational Study on Sars-COV 2 Population Hospitalized in the Italian Country

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04871685
Acronym
ECOVITA
Enrollment
950
Registered
2021-05-04
Start date
2020-10-18
Completion date
2021-05-03
Last updated
2021-05-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Respiratory Distress Syndrome

Keywords

lung ultrasound

Brief summary

Lung Ultrasound (LUS) has been revealing an extremely useful tool to identify and monitor complications from Sars-COV-2 disease. Recently, a research group has proposed a score, named LUS Score, able to optimize the use of this diagnostic technique. LUS Score is computed analyzing chest posterior and lateral spaces, considering the number of artefacts generated by the inflammed interstitium (B lines), the characteristics of the pleural line and the presence or not of consolidation areas. The comparison between LUS and chest tomography (CT), the current gold standard for the diagnosis of interstitial pneumonia by COVID-19, has confirmed from the preliminary data, the reliability of such technique. Hence, the validation on a really large sample size of the ultrasound tool performed by dedicated personnel with high expertise, may allow the validation both in the clinical practice and in emergency and ordinary wards.

Interventions

DIAGNOSTIC_TESTlung ultrasound

the patients underwent to a non invasive diagnostic exam to identify and monitor clinical conditions and onset of respiratory complications due to COVID-19

Sponsors

University of Campania Luigi Vanvitelli
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* men and women; * confirmed COVID19 diagnosis after nasal-oropharyngeal swab; * any symptom at hospitalization * any therapy * any pre-existing comorbidity

Exclusion criteria

* pregnant women * healthy subjects with other respiratory diseases different from COVID-19

Design outcomes

Primary

MeasureTime frameDescription
validation of lung ultrasound score6 monthsvalidation of lung ultrasound in the clinical practice of diagnosis of complications of low respiratory tracts during COVID-19

Secondary

MeasureTime frameDescription
Association of LUS score with clinical outcome6 monthsassessment of LUS score association with the clinical course of disease (final outcome, either discharged or in-hospital mortality
Association of LUS score with duration of hospitalization (days)6 monthsassessment of LUS score association with hospitalization days
Association of LUS score with respiratory support required6 monthsassessment of LUS score association with requirement of either sub-intensive or intensive therapy)

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026