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Predictive Factors COVID-19 Patients (MI-COVID)

19 de mayo de 2022 actualizado por: University of Milano Bicocca

Predictive Clinical Response Factors in COVID-19 Patients

This is a monocentric retro-prospective observational study that will be conducted on all COVID19 positive patients hospitalized at the S. Gerardo Hospital in Monza.

Descripción general del estudio

Estado

Retirado

Condiciones

Descripción detallada

BACKGROUND:

The Severe Acute Respiratory Syndrome-Coronavirus-2 (SARS-CoV-2) pandemic is severely testing the health systems of the most advanced countries. Clinicians are faced with a new pathology of an emerging virus. There is therefore an urgent need to collect real-time clinical data that informs about outcome predictive variables. Furthermore, there are currently no antiviral drugs approved for the treatment of SARS-CoV-2 infection, off-label therapies are being used with drugs already in use for other pathologies that have shown some efficacy in vitro, and some treatments obtained for compassionate use with other drugs that are being tested.

It is more than ever necessary to collect clinical practice data both retrospectively on the work done so far, and in a longitudinal perspective, and analyze them quickly to optimize current treatments and define protocols for the future. Having a good clinical data base also offers the possibility of collaborating with numerous international networks on translational research, which aims to correlate clinical data with virological and immunological data, aimed at the rapid identification of possible specific viral virulence factors, or particular immune structures of the guests who once again define the final clinical outcome.

STUDY DESIGN:

All COVID19 positive patients admitted to San Gerardo Hospital will be enrolled in the study.

After patient signs the informed consent, the following data will be collected:

  • birth data
  • sex
  • demographic data
  • comorbidity
  • blood chemistry data at the entrance

A series of variables will then be collected relating to the treatment procedure, the therapies, the team's choice to maximize the care ceiling in the individual patient and the entire clinical study of the patient.

STATISTICAL ANALISYS:

Central tendency and dispersion measurements will be used for descriptive analysis of continuous variables while absolute and relative frequencies will be used to describe categorical variables.

Tipo de estudio

De observación

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

      • Monza, Italia
        • ASST Monza-Ospedale San Gerardo

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Método de muestreo

Muestra no probabilística

Población de estudio

The study involves patients admitted to San Gerardo Hospital from March 1, 2020 to May 31, 2020. The minimum expected follow-up will be one year for all patients.

Given the nature of the study, no formal calculation of the sample size was made, nor was a sample size predefined. However, given the recruiting potential of the center which in March saw on average 30-60 hospitalizations due to SARS-CoV-2 per day, even considering a progressive decrease in access, it is assumed that the proportion of patients who will be included in the study will exceed 1000 units.

Descripción

Inclusion Criteria:

  • Patients 18 years old or above
  • Diagnosis of SARS-CoV-2 pneumonia

Exclusion Criteria:

  • Explicit refusal to participate in the study

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

Cohortes e Intervenciones

Grupo / Cohorte
Intervención / Tratamiento
Covid19 infection related patients
Patients admitted to COVID wards of the S. Gerardo Hospital of Monza, including Intensive Care wards.
Identify the risk factors for intra-hospital mortality in patients hospitalized in the COVID + hospital wards of the San Gerardo hospital and build a prognostic score through which it is possible to define a stratification that immediately guides the therapeutic choices and the intensity of care .

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Identify risk factors for intra-hospital mortality.
Periodo de tiempo: Until patient discharge from the hospital (approximately 1 year)
Identify risk factors for intra-hospital mortality in patients admitted to the COVID + hospital wards of San Gerardo hospital.
Until patient discharge from the hospital (approximately 1 year)
Identify risk factors to build a prognostic score.
Periodo de tiempo: Until patient discharge from the hospital (approximately 1 year)
Identify the risk factors to build a prognostic score through which it is possible to define a stratification that immediately guides the therapeutic choices.
Until patient discharge from the hospital (approximately 1 year)
Identify risk factors to build a prognostic score.
Periodo de tiempo: Until patient discharge from the hospital (approximately 1 year)
Identify the risk factors to build a prognostic score through which it is possible to define a stratification that immediately directs towards the right intensity of care.
Until patient discharge from the hospital (approximately 1 year)

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Predictive factors for the hospitalization duration.
Periodo de tiempo: Until patient discharge from the hospital (approximately 1 year)
Description of the predictive factors for the hospitalization duration.
Until patient discharge from the hospital (approximately 1 year)
Predictive factors for clinical status patients based on "Ordinal Scale for Clinical Improvement"
Periodo de tiempo: Until patient discharge from the hospital (approximately 1 year)
Description of the predictive factors for the clinical status of patients based on "Ordinal Scale for Clinical Improvement" defined by OMS (
Until patient discharge from the hospital (approximately 1 year)
Describe the anti-viral therapies used commonly in this emergency in terms of efficacy
Periodo de tiempo: Until patient discharge from the hospital (approximately 1 year).
Description of efficacy of the anti-viral therapies used today without particular restrictions, but on which solid clinical functioning tests are lacking.
Until patient discharge from the hospital (approximately 1 year).
Describe the anti-viral therapies used commonly used in this emergency in terms of safety
Periodo de tiempo: Until patient discharge from the hospital (approximately 1 year).
Description of safety of the anti-viral therapies used today without particular restrictions, but on which solid clinical functioning tests are lacking.
Until patient discharge from the hospital (approximately 1 year).
Monitor the clinical course of the disease in discharged patients.
Periodo de tiempo: 12 month after discharge
Description of the disease clinical course in patients 12 months after discharge (mortality, neurological, respiratory and cardiac outcomes).
12 month after discharge

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Publicaciones Generales

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

30 de abril de 2020

Finalización primaria (Anticipado)

1 de mayo de 2021

Finalización del estudio (Actual)

12 de mayo de 2022

Fechas de registro del estudio

Enviado por primera vez

4 de junio de 2020

Primero enviado que cumplió con los criterios de control de calidad

10 de junio de 2020

Publicado por primera vez (Actual)

11 de junio de 2020

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

26 de mayo de 2022

Última actualización enviada que cumplió con los criterios de control de calidad

19 de mayo de 2022

Última verificación

1 de mayo de 2022

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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