Table 3.
SN | Name of Trial | Antioxidant used | Aim of Study | Disease | Outcome |
---|---|---|---|---|---|
1 | BRONCUS | NAC | Effect on FEV1 | COPD | No effect. A reduction in lung over inflation in patients with severe COPD without inhaled glucocorticoids |
2 | Systematic Cochrane review of 23 randomized controlled trials | NAC (2 months of oral therapy) | Effect of NAC and antibiotics on number of days of disability | COPD | No effect on lung function. 29% decrease in exacerbations. Good reduction in days of disabibility (0.85 days/patient/month |
3 | Systematic Cochrane review of randomized controlled trials of 11 out of 39 reviewed trials | NAC | Used a validated score for evaluation of quality of each study | COPD | 9 trials showed prevention of exacerbations and 5 showed improvement in symptoms compared to 34.6% patients receiving placebos |
4 | A meta analysis of published trials | NAC (600 mg bid for 12 months) | To assess the possible prophylactic benefit of prolonged treatment Effect on H2O2 and TBARS in EBC |
COPD COPD |
23% decrease in acute exacerbation No change in TBARS, reduced H2O2 |
5 | EQUALIFE studies | Vectrine-erdosteine, thiol compound, 300mg bid for months | Exacerbation rate, hospitalization, lung function and quality of life in 124 patients | COPD | Decreased exacerbations and fewer days in hospital. No loss of lung function and improvement in health-related quality of life |
6 | PEACE study | Carbocysteine (carbocisteine) | Effect on rate of exacerbations | COPD | Long-term (one year) use of carbocysteine (1500 mg/day) produced reduction in numbers of exacerbations in patients with COPD |
BRONCUS = Bronchitis Randomized on N-acetyl-L-cysteine Cost Utility Study, FEV1 = Forced expiratory volume in 1 second, TBARS = Thiobarbituric acid reactive substances, NAC = N-acetyl-L-cysteine, EBC = Exhaled Breath Condensate.