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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04591704
Other study ID # UU-DM003
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 20, 2020
Est. completion date July 1, 2021

Study information

Verified date May 2021
Source Usak University
Contact Cevdet Duran
Phone 02762212121
Email drcduran@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

All hospitalised patients with COVID-19 who have positive RT-PCR for SARS-COV-2 will be included in the study. The patients will be divided into two groups, as diabetics and non-diabetics. The COVID-19 patients' medical records will be evaluated and compared in terms of the duration of hospitalization, the presence of lung involvement in Computerised Tomography, the need for intensive care unit and mortality rates in patients with and without diabetes.


Description:

All hospitalised patients with COVID-19 who have positive RT-PCR for SARS-COV-2 will be included in the study. The patients will be divided into two groups, as diabetics and non-diabetics. The diagnosis of diabetes mellitus will be extracted from the medical records and medical history of the patients hospitalised with COVID-19. The COVID-19 patients medical records will be evaluated and compared in terms of the duration of hospitalization, the presence of lung involvement in Computerised Tomography, the need for intensive care unit and mortality rates in patients with and without diabetes.


Recruitment information / eligibility

Status Recruiting
Enrollment 2000
Est. completion date July 1, 2021
Est. primary completion date October 15, 2020
Accepts healthy volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Patients hospitalized for COVID-19 Exclusion Criteria: - Patients with known malignancy - Pregnant patients

Study Design


Related Conditions & MeSH terms


Intervention

Other:
hospitalisation, necessity of ICU, mortality rate, lung involvement
hospitalisation, necessity of ICU, mortality rate, lung involvement

Locations

Country Name City State
Turkey Usak University Training and Research Hospital Usak

Sponsors (1)

Lead Sponsor Collaborator
Usak University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Duration of Hospitalisation The time between admission to hospital and discharge 1 year
Primary The need for ICU The admission of hospitalized patients to the intensive care unit. 1 year
Primary Mortality Mortality rates of patients 1 year
Primary Lung involvement The presence of lung involvement on thorax CT 1 year
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