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. 2016 May 25;2016:1656450. doi: 10.1155/2016/1656450

Table 1.

Clinical trials for evaluating the efficacy of antioxidant based pharmacotherapy in preventing the oxidative stress mediated myocardial tissue damage in cardiovascular diseases.

Drug Number of subjects Trial type Key findings Reference
N-acetylcysteine (NAC) 98 Double-blind, randomized clinical trial NAC prevented early remodeling by reducing the level of MMP-2 and MMP-9 [121]
52 Randomized clinical trial NAC decreased pump-induced oxidative stress during cardiopulmonary bypass [28]

Resveratrol 75 Triple-blinded, randomized, parallel, dose-response, and placebo-controlled trial Resveratrol-rich grape supplement improved the inflammatory and fibrinolytic status in patients who were on statins for primary prevention of CVD [122]

Rapeseeds 59 Randomized, double-blind, controlled, and crossover study Intake of a stabilized rapeseed oil enriched in cardioprotective micronutrients prevented the risk of cardiovascular diseases by improving the cholesterol profile and reducing LDL oxidation [123]

Flavonoids-epicatechin and quercetin 37 Randomized, double-blind, placebo-controlled, and crossover trial Epicatechin contributed to the cardioprotective effects of cocoa and tea by improving insulin resistance [124]

Pravastatin 10 Randomized clinical trial Oral pravastatin reloading before nonemergent coronary artery bypass grafting (CABG) significantly attenuated postoperative inflammation and systemic NO/iNOS concentrations and reduced the myocardial injury [125]

Magnesium 52 Randomized clinical trial The extensive treatment of the patients with magnesium influences the cellular response to ischemia and thus induces cardioprotection against oxidative stress [126]

Coenzyme Q10 51 Randomized clinical trial Coenzyme Q10 supplementation at 300 mg/day significantly enhances antioxidant enzymes activities and lowers inflammation in patients who have coronary artery disease during statin therapy [127]

Silymarin 102 Randomized trial The anti-inflammatory and antioxidant effects of silymarin treatment provided protection against reperfusion injury and inflammation after CABG surgery [128]
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