Actively Recruiting
Screening and Intervention for Subclinical Coronary Artery Disease in Patients With Type 2 Diabetes
Led by Per Løgstrup Poulsen · Updated on 2025-02-06
7300
Participants Needed
1
Research Sites
320 weeks
Total Duration
On this page
Sponsors
P
Per Løgstrup Poulsen
Lead Sponsor
O
Odense University Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
The investigators intend to perform a landmark study to answer whether a combined CVD screening and treatment strategy is beneficial for patients with type 2 diabetes (T2DM) without known cardiovascular disease (CVD) The investigators aim to answer the following main research questions: Do screening detected high-risk patients benefit of intensified medical treatment? Is it safe to de-intensify medical treatment among patients with a screening detected low risk of CVD? Does a CVD screening and treatment program improve patient reported health status? Cardiovascular risk remains high in patients with T2DM but unevenly distributed. Our current risk stratification strategies are far from optimal leading to both under- and over-treatment of patients. In recent years, noninvasive imaging of subclinical coronary artery disease by cardiac CT has improved considerably. This allows for easily accessible evaluations of coronary atherosclerosis burden and composition - exceptionally strong imaging biomarkers of future cardiovascular disease. An increasing amount of data suggests that cardiac CT may permit better risk stratification in patients with T2DM. At the same time, the pharmaceutical treatment of T2DM has changed with several new and expensive drug classes, each individually documented to reduce the risk for new or recurrent cardiovascular events. Thus, these new drugs may improve outcome in high-risk patients, whereas they may be wasteful and only lead to side effects in low-risk patients. In the Inten-CT study, the investigators combine these two pivotal developments. The investigators intend to improve risk stratification of patients with T2DM by use of cardiac CT and, based on this knowledge, the investigators wish to investigate if upgraded medical treatment in the high-risk population is beneficial and if de-intensified treatment in the low-risk population is safe. As a secondary aim, the investigators wish to investigate if such a strategy improves patient reported health status. These aims are in agreement with one of the important health indicators from The Danish College of General Practitioners: "We find and treat the patients and let the healthy stay healthy". The investigators intend with this strategy to improve not only cardiovascular outcome among patients with T2DM, but also their quality of life. The Inten-CT study is an investigator-initiated open-label event-driven randomized controlled trial including patients with T2DM stratified according to screen detected coronary artery calcification. The investigators expect inclusion of 7300 patients in 2 years and a mean follow-up period of 5 years.
CONDITIONS
Official Title
Screening and Intervention for Subclinical Coronary Artery Disease in Patients With Type 2 Diabetes
Who Can Participate
Eligibility Criteria
You may qualify if you...
- New or former diagnosis of Type 2 diabetes according to WHO
- Age between 55-69 years (men) and 60-74 years (women)
- Signed declaration of consent
You will not qualify if you...
- Previous history of cardiovascular disease including myocardial infarction, coronary intervention, heart failure, stroke, or peripheral artery disease
- Allergies or contraindications to both SGLT2 inhibitors and GLP-1 analogues
- Signs of critical cardiac disease such as >50% stenosis of left main coronary artery or left ventricular ejection fraction below 30%, or CAC >1000 if CT angiography unavailable
- Expected life duration less than 1 year for any reason
AI-Screening
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Trial Site Locations
Total: 1 location
1
Odense University Hospital
Odense, Denmark, 5000
Actively Recruiting
Research Team
K
Kristian L Funck, MD PhD
CONTACT
P
Per L Poulsen, Professor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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