A Randomized, Open-label, Clinical Trial Evaluating the Anti-atherosclerotic Efficacy of Selected Antidiabetic Drugs in Patients With Coronary Artery Disease and Pre-diabetes

Status: Recruiting
Location: See location...
Intervention Type: Drug, Behavioral
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

The purpose of the study is to compare the anti-atherosclerotic efficacy of oral treatment with a GLP-1 analogue (semaglutide) or an SGLT-2 (so-called flozin) inhibitor (dapagliflozin) versus routine treatment (metformin) in patients with pre-diabetes and diagnosed coronary artery disease at 24 months. The diagnosis of coronary artery disease will be defined as the presence of coronary atherosclerosis confirmed by coronary artery computed tomography (coronary CT). The study will evaluate the effect of treatment with flozin vs. semaglutide compared to treatment with metformin on the progression/regression of coronary atherosclerosis, change in plaque character, and control of cardiovascular risk factors.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
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• Age 18 - 80

• Diagnosed coronary artery disease (coronary artery stenosis of at least 20% with a reference diameter of \>2.5 mm or status after percutaneous coronary revascularization procedure found on coronary CT scan)

• Coronary CT scan performed \<3 months after inclusion in the study, at least of good quality

• Pre-diabetic status defined as fasting blood glucose 100-125 mg% or Hba1c 5.70-6.49% (measurement documented at the screening/randomization appointment or within 30 days prior to the screening/randomization appointment) or documented, positive result of an oral glucose load test (fasting blood glucose 100-125 mg% and 140-199 mg% 2h after a 75 g oral glucose load) performed up to 30 days before the screening/randomization appointment

• Stable treatment and control of cardiovascular risk factors, including dietary and lifestyle management for at least 4 weeks

• Willing and able to give informed consent to participate in the study

• Willing and able, according to the researcher, to comply with all the requirements of the study

Locations
Other Locations
Poland
National Institute of Cardiology, Department of Coronary Artery and Structural Heart Diseases
RECRUITING
Warsaw
Contact Information
Primary
Jan Henzel, MD, PhD
jhenzel@ikard.pl
+48 22 343 43 42
Backup
Kinga Kotlinska
kkotlinska@ikard.pl
+48 22 343 40 88
Time Frame
Start Date: 2025-07-10
Estimated Completion Date: 2029-08-01
Participants
Target number of participants: 300
Treatments
Experimental: DAPAGLIFLOZIN
Dapagliflozin + OMT \& Lifestyle Intervention
Experimental: SEMAGLUTIDE
Semaglutide + OMT \& Lifestyle Intervention
Active_comparator: METFORMIN
Metformin + OMT \& Lifestyle Intervention
Related Therapeutic Areas
Sponsors
Collaborators: Medical Research Agency, Poland
Leads: National Institute of Cardiology, Warsaw, Poland

This content was sourced from clinicaltrials.gov