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To study the effect of atorvastatin treatment on vascular uptake of 68Ga-DOTATATE in patients with Type 2 Diabetes.
Full description
Well controlled patients with type 2 diabetes, who are statin naïve, will undergo atorvastatin treatment. Before and after treatment, patients will undergo a 68Ga-DOTATATE PET/CT, to evaluate the effect of treatment on vascular inflammation.
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Inclusion criteria
Exclusion criteria
History of cardiovascular disease (previous CV-event (MI / stroke) or known coronary artery disease (including acute coronary syndrome).
History of chronic kidney disease stage 3b - 5, defined as a CKD-EPI value of < 45 ml/min/1,73m2
Malignant diseases or any clinically significant medical condition that could interfere with the conduct of the study in the opinion of the investigator.
Chronic or recent (< 1 month) infections and/or clinical signs of acute infection.
History of auto-immune diseases.
Standard contra-indications to 68Ga-Dotatate PET, and CT based on physicians experience and current practices.
Inability or unwillingness to comply with the protocol requirements, or deemed by investigator to be unfit for the study.
Planned radiation exposure in the next year due to participation in a research project with radiation exposure or for clinical reasons.
Elevated liver enzymes (> 2 ULN of liver transaminases), acute liver failure or known liver disease.
Prior medium to severe statin-related side effects or statin related hypersensitivity, i.e.
(severe) muscle pains with and/or without myopathy .
The concomitant use of statin contra-indicated drugs, including the use of CYP3A4 inhibitors (i.e. erytromycin, dilthiazem, amiodaron, verapamil, fluconazole, ciclosporin, stiripentol, itraconazol, ketoconazol, voriconazol, posaconazol, clarithromycin, ..), systemic use of fusidic acid and ciclosporin.
Any contra-indications to the use of statins.
Primary purpose
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Interventional model
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24 participants in 1 patient group
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Data sourced from clinicaltrials.gov
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