rct
    2005
    High Quality

    Effects of N-acetylcysteine on outcomes in chronic obstructive pulmonary disease (Bronchitis Randomized on NAC Cost-Utility Study, BRONCUS): a randomised placebo-controlled trial

    Decramer M, Rutten-van Molken M, Dekhuijzen PN, Troosters T, van Herwaarden C, Pellegrino R, van Schayck CP, Olivieri D, Del Donno M, De Backer W, Lankhorst I, Ardia A

    Published in The Lancet

    Methodology

    Three-year multicentre randomised placebo-controlled trial of N-acetylcysteine 600 mg once daily in patients with COPD, with rate of decline in FEV1 and exacerbation rate as co-primary endpoints.

    Key Findings

    N-acetylcysteine did not slow the decline in FEV1 and did not reduce exacerbation rates overall, though a subgroup not using inhaled corticosteroids showed fewer exacerbations.

    Conclusions

    Once-daily N-acetylcysteine was ineffective for disease progression in COPD.

    Limitations

    Dose may have been too low; high background inhaled corticosteroid use may have masked benefit; subgroup finding exploratory.

    Supplements Studied

    N-acetylcysteine did not slow the decline in FEV1 and did not reduce exacerbation rates overall.

    Outcomes Measured

    N-acetylcysteine did not reduce the yearly decline in FEV1 or the exacerbation rate overall.

    Related Health Concerns

    Study Details

    Year:2005
    Sample Size:523
    Duration:156 weeks
    Quality Score:9/10

    Disclosures

    Funding

    Zambon Group with European academic centres

    This information is for educational purposes only. Always consult a healthcare professional before starting any supplement regimen.