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The Severity of COVID 19 in Diabetes and Non-diabetes Patients (COVID19)

Study on Characteristics and Prognosis of Diabetes and Non Diabetes Patients With COVID 19 Among Southern Indian Population

There were 83,85,440 confirmed cases of COVID-19 worldwide with a mortality rate of 5.4% according to the situation report of the World Health Organisation on June 19, 2020. In India there were 3,95,048 confirmed cases of COVID-19 with a mortality rate of 3.3%. In Tamil Nadu there were 54,449 confirmed cases of COVID-19 with a mortality rate of 1.2% according to the report of Ministry of Health and Family Welfare, Government of India on June 19, 2020.

COVID-19 infection is a double challenge for people with diabetes. India has a large number of persons with diabetes (more than 77 million). Recent studies have reported rising prevalence both in the urban and rural populations. The incidence of type 2 diabetes (T2D) also shows an increasing trend in the last few decades. Mortality seems to be threefold higher in people with diabetes when COVD-19 coexists when compared with mortality due to COVID-19 without comorbidities.

Yang et al noted that among 52 intensive care patients who had COVID 19 infection, 22% had diabetes among the non-survivors. In a study of 173 patients with severe disease, 16.2% had diabetes, and in another study of 140 hospitalized patients, 12% had diabetes. Li et al compared intensive care and non-intensive care patients who had COVID-19. They showed a twofold increase in the incidence of diabetes in intensive care patients.

In addition to diabetes; the other common co-morbidities present in COVID 19 patients were hypertension (20%), cardiovascular disease (16%), and lung disease (6%). In this context, patients with diabetes have been listed as people with higher severity for COVID-19 by several health authorities. However, precise data regarding patients with and without diabetes having COVID-19 infection are still lacking. Moreover, the relationship between diabetes and the severity of COVID-19 remains unknown. In this study, we intend to identify the disease severity and mortality in people with and without diabetes admitted for COVID-19 in southern India.

Descripción general del estudio

Estado

Desconocido

Descripción detallada

The following data from a person tested positive for COVID 19 and hospitalized will be collected. Patient's anthropometry (height in cms, weight in kgs and body mass index in kg/m2), blood pressure, symptoms of COVID-19 (fever, fatigue, cough, cephalalgia, dyspnoea, rhinitis, pharyngeal symptoms, ageusia, anosmia, digestive disorders), history of smoking, hypertension, dyslipidemia, microvascular (retinopathy, nephropathy and neuropathy), macrovascular (coronary artery disease, cerebrovascular disease and peripheral vascular disease) complications and other co morbid conditions will be recorded. Fasting blood glucose, HbA1c and any other relevant investigations if available and treatment for COVID-19 and other co morbid conditions will be recorded.

Details of patients developing new symptoms, shifted to ICU, intubated or died during the course of treatment will be recorded. Appearance of any complication during the stay at hospital will be recorded. The changes in the treatment pattern during the course of the disease will also be noted.

The registry will be fully anonymised and statistician will have no access to patients' personal identifiers. All "investigators" will have to register before entering data in the registry. Data about clinical observations for the individual patient will be entered by clinicians or by authorised research personnel of the care team in the web registry.

Patients' name, date of birth, date of death, residential postal code, hospital number will be fully anonymised at source. In no circumstances, patients' identifiable data be available to anyone outside their own care teams or authorised local administration/research personnel. Patient data will not at any stage will be in identifiable form by the registry managers. The data to be collected from the patients are mentioned in the visit chart.

Tipo de estudio

De observación

Inscripción (Anticipado)

1050

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

    • Tamil Nadu
      • Chennai, Tamil Nadu, India, 600014
        • Orthomed Hospital
      • Chennai, Tamil Nadu, India, 600024
        • Medway Hospital
      • Chennai, Tamil Nadu, India, 600035
        • Venkateswara Hospital
      • Chennai, Tamil Nadu, India, 600044
        • Dr. Rela Institute & Medical Center

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 a 99 años (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Método de muestreo

Muestra no probabilística

Población de estudio

COVID 19 positive patients with or without diabetes

Descripción

Inclusion Criteria:

  • >18 yrs male or female
  • COVID-19 positive

Exclusion Criteria:

  • COVID 19 Negative
  • New-onset Diabetes with covid-19 infection

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
COVID 19 positive patients without diabetes
COVID 19 positive patients with diabetes

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Severity of COVID 19 among people with and without diabetes
Periodo de tiempo: Up to 1 month
To identify the disease severity and outcome among people with and without diabetes hospitalized for COVID 19 virus infection
Up to 1 month

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Number of patients who were in ICU
Periodo de tiempo: Up to 1 month
Number of patients who were in ICU
Up to 1 month
Number of patients who had tracheal intubation
Periodo de tiempo: Up to 1 month
Number of patients who had tracheal intubation
Up to 1 month
Number of patients who had respiratory complication
Periodo de tiempo: Up to 1 month
Number of patients who had respiratory complication
Up to 1 month
Number of death
Periodo de tiempo: Up to 1 month
Number of death
Up to 1 month
Correlation of BMI with complications, tracheal intubation and mortality
Periodo de tiempo: Up to 1 month
Correlation of BMI with complications, tracheal intubation and mortality
Up to 1 month
Length of hospital stay
Periodo de tiempo: Up to 1 month
Length of hospital stay
Up to 1 month

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: Ambady Ramachandran, M.D,PhD,DSc, President

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 (Anticipado)

16 de noviembre de 2020

Finalización primaria (Anticipado)

16 de febrero de 2021

Finalización del estudio (Anticipado)

16 de mayo de 2021

Fechas de registro del estudio

Enviado por primera vez

15 de noviembre de 2020

Primero enviado que cumplió con los criterios de control de calidad

17 de noviembre de 2020

Publicado por primera vez (Actual)

18 de noviembre de 2020

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

18 de noviembre de 2020

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

17 de noviembre de 2020

Última verificación

1 de noviembre de 2020

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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