crossover
    1998
    High Quality

    Prospective evaluation of vitamin E for hot flashes in breast cancer survivors

    Barton DL, Loprinzi CL, Quella SK, Sloan JA, Veeder MH, Egner JR, et al.

    Published in J Clin Oncol, Vol. 16 (2), pp. 495-500

    Methodology

    Placebo-controlled, randomised, double-blind crossover trial in breast cancer survivors with hot flashes: after a baseline week, 4 weeks of vitamin E 800 IU daily and 4 weeks of identical placebo, in random order, with daily hot flash diaries.

    Key Findings

    In the 105 women who finished the first period, hot flash frequency fell by 25% with vitamin E and 22% with placebo (P = .90). The crossover analysis found about one fewer hot flash per day with vitamin E than placebo (P <= .05). At the end, 32% preferred vitamin E and 29% placebo; no toxicity was seen in 120 women.

    Conclusions

    Vitamin E produced a statistically significant but clinically marginal reduction in hot flashes.

    Limitations

    Short treatment periods (4 weeks each); breast cancer survivors only, so results may differ in other women; large placebo response.

    Supplements Studied

    Vitamin E
    Vitamin

    the clinical magnitude of this reduction was marginal

    Outcomes Measured

    the clinical magnitude of this reduction was marginal

    Related Health Concerns

    Study Details

    Year:1998
    Sample Size:120
    Duration:8 weeks
    Quality Score:7/10

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