Atorvastatin Treatment to Attenuate the Progression of Cardiovascular Disease: Prospective, Randomized, Controlled Study
Overview
- Phase
- Phase 3
- Intervention
- atorvastatin
- Conditions
- Vascular Calcification
- Sponsor
- Ercan OK
- Enrollment
- 446
- Locations
- 1
- Primary Endpoint
- progression of coronary artery calcification score
- Status
- Completed
- Last Updated
- 12 years ago
Overview
Brief Summary
This prospective, randomized, controlled study aims to investigate the effects of atorvastatin treatment in hemodialysis patients concerning progression of coronary artery calcification, progression of carotid artery intima-media thickness, endothelial function, and inflammation.
Detailed Description
The effects of statin treatment on coronary artery calcifications, carotid artery intima-media thickness, and endothelial functions have never been investigated in hemodialysis patients. Regarding inflammation, the present data in hemodialysis patients are derived from small studies with short follow-up. We postulate that atorvastatin would reduce progression of coronary calcification and carotid artery intima-media thickness, decrease inflammation, and improve endothelial function. In this prospective, controlled, randomized study, four hundred forty-six prevalent hemodialysis patients who meet inclusion and exclusion criteria will be randomized to atorvastatin (20 mg/day in first month; increased to 40 mg/day afterwards) and placebo arms (each arm consists of 223 patients), after completion of baseline investigations. Randomization will be performed with random permuted blocks and will be stratified according to dialysis center, age, sex, diabetic status, duration of dialysis, high flux dialyser use, and dialysate calcium level. Follow-up period will be twelve months. It is estimated that 446 patients would provide 90% power with a two-sided, alpha error rate of 5%, of detecting a significant difference between treatment arms. Dropout rate is expected to be 20%, not to be replaced.
Investigators
Ercan OK
professor
Ege University
Eligibility Criteria
Inclusion Criteria
- •aged between 18 and 80 years
- •on maintenance bicarbonate hemodialysis scheduled thrice weekly, at least 12 hours/week
- •willingness to participate to the study with a written informed consent
Exclusion Criteria
- •to have serious life-limiting co-morbid situations, namely active malignancy, active infection, end-stage cardiac, pulmonary, or hepatic disease
- •to be scheduled for living donor renal transplantation
- •pregnancy or lactating
- •history of coronary bypass grafting, acute myocardial infarction or unstable angina pectoris confirmed by angiography within three months of randomization
- •presence of an absolute indication to use lipid lowering drug or an absolute contraindication for lipid lowering therapy according to investigator's opinion
- •history of statin sensitivity or adverse reaction to statins
- •receiving any lipid-lowering agents within three months of randomization
- •uncontrolled hypothyroidism defined as TSH level higher than 1.5 times of upper limit
- •receipt of any investigational drug within 30 days before randomization
- •inability to tolerate oral medication or history of significant malabsorption
Arms & Interventions
Statin
Atorvastatin 40 mg/day
Intervention: atorvastatin
Placebo
placebo
Intervention: placebo
Outcomes
Primary Outcomes
progression of coronary artery calcification score
Time Frame: one year
progression of carotid artery intima-media thickness
Time Frame: one year
changes in the level of hsCRP
Time Frame: one year
Secondary Outcomes
- changes in the endothelial function(one year)
- changes in the level of hsCRP(one year)