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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04780373
Other study ID # prot. N. 71726
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 1, 2020
Est. completion date December 1, 2020

Study information

Verified date April 2021
Source University of L'Aquila
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the study is to define the clinical and biochemical parameters that characterize COVID-19 patients with a negative prognostic evolution. Our clinical score will be capable to recognize patient with favorable prognosis or patient with poor prognosis by statistical data analysis.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date December 1, 2020
Est. primary completion date December 1, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - patients over 18 and symptomatic and positive for COVID-19 by polymerase chain reaction assay for rhino-pharingeal swab Exclusion Criteria: - Under 18

Study Design


Related Conditions & MeSH terms


Intervention

Other:
data collection
clinical data collection

Locations

Country Name City State
Italy University of L'Aquila L'Aquila

Sponsors (1)

Lead Sponsor Collaborator
University of L'Aquila

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Data collection of clinical and demographical parameters of patients affected by COVID-19 Data about sex, age, symptom start date, vital parameters, comorbidity, symptoms, hematochemicals blood tests, therapy, oxygen support, radiology, condition evaluation will be manual collected. 8 months
Secondary Application of statistical analysis on data of patients affected by COVID-19 The collected data will be analyzed through descriptive statistics analysis, ROC curves, regression analysis, and Machine Learning techniques to predict the prognosis of patients affected by COVID-19. 2 months