crossover
    2018

    Daily intake of Mucuna pruriens in advanced Parkinson's disease: A 16-week, noninferiority, randomized, crossover, pilot study

    Cilia R, Laguna J, Cassani E, Cereda E, Raspini B, Barichella M, Pezzoli G

    Published in Parkinsonism & Related Disorders

    Methodology

    Randomized crossover noninferiority pilot trial comparing Mucuna pruriens seed powder with marketed levodopa/carbidopa in Parkinson's patients with motor fluctuations

    Key Findings

    In those who tolerated MP, clinical response was similar to levodopa/carbidopa on all efficacy outcomes, but 50% discontinued MP early due to gastrointestinal side-effects or worsening motor performance.

    Conclusions

    Benefit of Mucuna pruriens was limited by tolerability rather than efficacy; larger parallel-group studies are needed to define formulation and dosing.

    Limitations

    Very small pilot sample, high dropout, open switch from levodopa/carbidopa, single-centre

    Supplements Studied

    In those who tolerated MP, clinical response to MP was similar to LD/CD on all efficacy outcome measures.

    Outcomes Measured

    In those who tolerated MP, clinical response to MP was similar to LD/CD on all efficacy outcome measures.

    Study Details

    Year:2018
    Sample Size:14
    Duration:16 weeks
    Quality Score:6/10

    Disclosures

    Funding

    Not reported

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