Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Medical University of Vienna
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Diabetes patients:
Men and women aged over 18 years.
subjects with both hypercholesterolemia and normal lipid profile will be included.
Diabetes type I or type II. Only patients with no signs of diabetic retinopathy (level 1) or patients with mild or moderate diabetic retinopathy will be included. Level of diabetic retinopathy will be assessed according to the modified Airlie House classification (1991).
Normal laboratory values unless the investigator considers an abnormality to be clinically irrelevant.
Normal findings in the medical history and physical examination unless the investigator considers an abnormality to be clinically irrelevant.
-Normal ophthalmic findings, except diabetic retinopathy as described above, ametropia \< 6 Dpt.
Glaucoma patients:
Men and women aged over 18 years.
Subjects with both hypercholesterolemia and normal lipid profile will be included.
Open angle glaucoma defined as pathological optic disc appearance and characteristic visual field loss. Visual field loss is defined as having a glaucoma hemifield test outside normal limits and/or a CPSD with P \< 0.05 (Keltner et al. 2003).
Normal laboratory values unless the investigator considers an abnormality to be clinically irrelevant.
Normal findings in the medical history and physical examination unless the investigator considers an abnormality to be clinically irrelevant.
Normal ophthalmic findings, except glaucoma as described above, ametropia \< 6 Dpt.
sufficiently controlled intraocular pressure.
You may not be if
Abuse of alcoholic beverages, participation in a clinical trial in the 3 weeks preceding the study.
Symptoms of a clinically relevant illness in the 3 weeks before the first study day.
Previous or current treatment with statins.
Current treatment with fibrates.
History or presence of renal failure, creatine kinase (CK) and lactic dehydrogenase (LDH) above normal levels.
History or presence of hepatic dysfunction, including increase of liver enzymes.
Patients with known hypersensitivity to the study drug or any ingredients.
Patients with or with a history of myopathy.
Systemic treatment with oral anticoagulants except low dose aspirin.
Blood donation during the previous 3 weeks.
Ametropia of 6 or more than 6 dpt.
Presence of intraocular pathology other than non proliferative diabetic retinopathy for cohort I and glaucoma for cohort II.
Ophthalmological surgery (including argon laser trabeculoplasty (ALT), trabeculectomy, deep sclerectomy) within the last 6 months before the study.
