COVID-19 Disease Clinical Trial
Official title:
Diabetes and COVID-19 in Tunisia (CoviDTUN)
NCT number | NCT05603130 |
Other study ID # | CoviDTUN |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | March 23, 2022 |
Est. completion date | October 17, 2022 |
Verified date | October 2022 |
Source | Les Laboratoires des Médicaments Stériles |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
CoviDTUN is a multicenter observatory set up by a steering committee to determine the presentation and evolution of diabetes in COVID-19 and study its pathogenesis. The observatory comprises a dataset consisting of routinely collected clinical information anonymously to be entered by the investigator as a participating clinician/researcher. The study will be an opportunity to understand the relationship between COVID-19 and diabetes, to enrich Tunisian data on diabetic and de novo diabetic patients who have contracted COVID-19 and to evaluate the prognostic severity factors for better management of these patients.
Status | Completed |
Enrollment | 811 |
Est. completion date | October 17, 2022 |
Est. primary completion date | June 30, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Diagnosis of COVID-19 infection confirmed by an evocative clinical picture according to INEAS score or a positive polymerase chain reaction [PCR] test and/or chest CT specific radiological signs and/or a rapid diagnostic antigen test. - Diabetes known before COVID-19 (known diabetes patient before COVID-19: Diabetic patient before COVID-19: History in medical record and/or presence of antidiabetic therapy and/or HbA1c = 6.5%). or - De novo diabetes (the de novo diabetic patient is defined as: Fasting blood glucose = 1.26 g/L (7mmol/L) or postprandial blood glucose = 2g/L (11.1 mmol/L) within 2 weeks of COVID-19 infection, no history of diabetes before the COVID-19 episode)). Exclusion criteria: - children - pregnant women |
Country | Name | City | State |
---|---|---|---|
Tunisia | Autoimmune diseases research unit UR17DN02, Department of Internal Medicine at the Military Hospital of Tunis | Tunis |
Lead Sponsor | Collaborator |
---|---|
Les Laboratoires des Médicaments Stériles |
Tunisia,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Effectiveness of patients with COVID-19 who have developed de novo diabetes. | The de novo diabetic patient is defined as follows: Fasting blood glucose = 1.26 g/L (7mmol/L) or postprandial blood glucose = 2g/L (11.1 mmol/L) within 2 weeks of COVID- 19 infection, no history of diabetes before the COVID-19 episode. | 3 months | |
Secondary | Demographic characteristics of diabetic patients | age, weight, gender, BMI, age of diabetes, diabetes treatments, type of diabetes, diabetes complications, comorbidities (hypertension, heart disease, dyslipidemia), vaccination status (number of doses, type of vaccine), associated treatments, hospitalization, evolution (use of respiratory support, cure, death following COVID-19 infection in diabetic and non-diabetic patients). | 3 months |
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