The Natural History of Hospitalized COVID-19 Patients — STORM  

Sars-CoV2 Clinical Trial

Official title: Observational Cohort Study on the Natural History of Hospitalized SARS-COV-2 Patients: the STORM Trial

Status Recruiting

Clinical Trial Summary

This is an observational study. The aim is to describe the natural history and clinical evolution over time of hospitalized patients affected by Severe Acute Respiratory Syndrome-Coronavirus-2 (SARS-COV-2) infection, including the genetic pathology of the disease and improve therapeutic procedures.

Clinical Trial Description

BACKGROUND: As of the end of February 2020, the ASST of Monza, with its two hospital wards of Monza and Desio, has treated 1433 COVID+ patients, of which 507 have currently been discharged (35.4%) and 206 (14%) transferred to other Low-intensity care facilities. The importance of observational studies is now known in many fields of medicine and the "real life" data produced have become an integral part of the authorization dossiers by the competent authorities to govern the introduction of new drugs: in particular, in a disease such as that from COVID-19 in which the absence of specific anti-viral therapies prevents an "ad hoc" cure, it becomes fundamental to identify and validate systems of stratification of the risk of fatal events, in order to optimize health intervention measures. METHODS AND STUDY DESIGN: The study protocol provides the collection of clinical, diagnostic and therapeutic and laboratory data consistent with the objectives of the study (CORE DATA SET) to which other specific protocols and relative data will connect (DATABASE "leaf"). The data collection will be performed on eCRF (RedCap platform) and the database will have the "stem and leaf" structure, compatible with WHO indications regarding pandemic data collection. CORE DATA SET: The protocol presents two important aspects of innovation in its formulation and design: 1. The "stem and leaf" structure will allow to collect all the core data of the study ("stem") capable of describing the primary objective, that is the natural history of the disease, thus providing an important contribution to knowledge, currently very scarce , the evolution of the disease; 2. the extreme heterogeneity of the pathology itself, the methods of spreading the contagion and the problematic treatment of some particular patient populations, however impose the description and the potential validation, not only in the context of subgroup analyzes, but in studies dedicated, of the data collected The "stem and leaf" design could therefore answer both questions. BIOLOGICAL SAMPLE COLLECTION: The biological research areas that the protocol proposes to pursue are listed below: 1. Study of genetic determinants of COVID-19 infection with the aim of identifying the bases of the different susceptibility in relation to age, sex and presence of co-morbidity; 2. Study of the repertoire of B and T lymphocyte receptors and identification of the virus-specific sequences of the T receptor for the antigen with the aim of identifying the component of the viral genome relevant to the immune response with possible relapses for the development of a vaccine; 3. Study of the activation of the inflammosome responsible for the abnormal and severe inflammatory response characteristic of patients with COVID-19 infection and serious lung complications with the aim of identifying possible specific targets of intervention against one or more inflammatory cytokines; 4. Study of the serological response during the acute phase of the disease and convalescence with the aim of defining the possible state of protection from the disease itself; 5. Study of the proteome with the aim of defining biomarkers capable of evaluate the risk of progression. STATISTICAL ANALYSIS: For each specific protocol, the study design and statistical data analysis plan will be formulated according to the specific objectives. In general, in addition to the descriptive methods, statistical regression models and methods for the definition of prognostic scores will be used, with relative cross-validation, which will allow to evaluate both binary and survival outcomes (in a broad sense, of events considered in time). ;

Related Conditions & MeSH terms

• Sars-CoV2

• NCT number: NCT04424992
• Study type: Observational
• Source: University of Milano Bicocca
• Contact: Paolo Bonfanti
• Phone: +39 039 233 9310
• Email: paolo.bonfanti@unimib.it
• Status: Recruiting
• Start date: February 28, 2020
• Completion date: May 2023