Cardiovascular Diseases Clinical Trial
— TOSCANAOfficial title:
Towards Optimal Screening and Management of Coronary Artery Disease in Diabetes: TOSCANA Study
NCT number | NCT05314140 |
Other study ID # | 2021-01 |
Secondary ID | |
Status | Not yet recruiting |
Phase | |
First received | |
Last updated | |
Start date | June 1, 2022 |
Est. completion date | June 30, 2026 |
There are currently only few data on the coronary artery calcium score in patient with diabetes in France, and the diagnostic and therapeutic attitudes towards a high coronary artery calcium score are not standardized and depend on clinical practices, which may vary from one center to another. The proposed multicenter prospective study would provide a better understanding of the epidemiological particularities of the coronary artery calcium score in French diabetics, refine the indications for better performance of the examination, and compare attitudes when this score is high.
Status | Not yet recruiting |
Enrollment | 2000 |
Est. completion date | June 30, 2026 |
Est. primary completion date | June 30, 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility | Inclusion Criteria: - Coronary asymptomatic patient - Patient with type 2 diabetes and aged 50 to 70 or - Patient with type 2 diabetes for more than 10 years and aged 18 to 50 or - Patient with type 1 diabetes for more than 20 years and aged > 35 - Coronary artery calcium score evaluation planned Exclusion Criteria: - Patients who already have a clinical history of coronary disease - Patients with other peripheral arterial disease - Patients with clinical suspicion of coronary artery disease - Patients with progressive cancer - Patients with serious chronic conditions with an estimated life expectancy < 3 years. - Pregnant, lactating, or pre-menopausal women without a recent negative pregnancy test available. - Patients under guardianship or curator or placed under justice safeguard - Patients who do not benefit from the social security scheme, or any equivalent scheme - Patients refusing or being linguistically or psychologically unable to sign the informed consent form Participation in another biomedical research protocol is permitted |
Country | Name | City | State |
---|---|---|---|
France | CHU de Bordeaux | Bordeaux | |
France | CHU de Limoges | Limoges | |
France | CHU de Nice | Nice | |
France | Hôpital Lariboisière, APHP | Paris | |
France | Hopital Saint Antoine | Paris | |
France | CHU de Poitiers | Poitiers | |
France | CHU de la Réunion | Saint-Denis | |
France | Centre de Cardiologie de Thionville | Thionville | |
France | CHU de Tours | Tours |
Lead Sponsor | Collaborator |
---|---|
French Cardiology Society | CEBIMER, Novo Nordisk A/S |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Proportions of diabetic patients with high coronary artery calcium score | Number of patient with diabetes having a coronary artery calcium score higher than 400 | day 1 | |
Secondary | Proportion of patients having a coronary exploration | Number of patient with high coronary artery calcium (>400) score having a coronary exploration compared with patient with low coronary artery calcium score (<400) | 6 months | |
Secondary | Proportion of patients having a myocardial revascularization | Number of patient with high coronary artery calcium score (>400) having a myocardial revascularization compared with patient with low coronary artery calcium score (<400) | 3 months | |
Secondary | Description of adverse events regarding to the coronary artery calcium score | Calculation of number and type of cardiovascular adverse event within patient with high coronary artery calcium score (>400) or low coronary artery calcium score (<400) | 6 months / 12 months / 18 months / 24 months / 30 months / 36 months / 42 months / 48 months |
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