Alpha Lipoic Acid Against Cardiovascular Events in Patients With Haemodialysis

Hemodialysis Complication

alpha-lipoic acid, Cardiovascular events, Hemodialysis

Evaluate the association between possible benefit effects of oral administration of alpha lipoic acid by patients with hemodialysis and the possible reduction in cardiovascular events (CVEs); using Advanced glycation end products (AGEs) as a measure to assess endothelium function which correlate with CVEs.

Study design: double blind, Parallel, Randomized, Prospective, Controlled study. Setting: Nephrology Department, Dialysis units, Ain Shams University Hospitals, Ain Shams University, Cairo, Egypt. Sample size: 36 patients with end-stage renal disease (ESRD) receiving dialysis treatment will be enrolled in the study and the patients will be identified by coded numbers to maintain the privacy. Patients will be randomized into two groups each group includes 18 patients: Control Group: 18 patients will receive their standard therapy only. Tested Group: 18 patients will receive alpha-lipoic acid (thiotacid R) product with their standard therapy. Materials: Thiotacid R 600 mg tablet. Each tablet contains: Thioctic acid (Alpha-lipoic acid) 600 mg; a product of EVA pharma, Cairo, Egypt. Methods: All Patients will be subjected to the following: 1. Informed consent 2. Demographics and history taking: Using Patient Data sheet 3. Laboratory evaluation including: A- Routine laboratory measurements as hemoglobin, calcium, phosphate, and albumin will be determined. The assessment will be done in 2 occasions: i. At Baseline (before the beginning of the treatment) for all groups ii. After 3 months of addition of alpha lipoic acid to their standard therapy for the tested group. 4. Follow up: A- During-treatment follows up of the patients: All patients will be followed up during the study for treatment tolerability by assessing adverse effects, and compliance to drug regimen. Drug regimen: - the patients in tested group will administered Thiotacid 600 mg; orally once daily for 3 months as add on the standard therapy that are receiving. Patients will be interviewed weekly through face to face contact with the clinical pharmacist regarding treatment tolerability, and through telephone calls in between these weekly meetings. B- Post-treatment follows up of the patients: All patients in control group will be followed up clinically after 3 months from the start of the study and all laboratory examinations will be carried out. All patients in tested group will be followed up clinically after 3 months from the start of treatment and all laboratory examinations will be carried out.

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