rct
    1985

    Evening primrose oil (Efamol) in the treatment of Raynaud's phenomenon: a double blind study

    Belch JJ

    Published in Thrombosis and Haemostasis

    Methodology

    Double-blind placebo-controlled trial of evening primrose oil over 8 weeks in patients with Raynaud's phenomenon, with attack diaries plus objective measures of digital blood flow and cold challenge.

    Key Findings

    In 21 patients with Raynaud's phenomenon, evening primrose oil (Efamol) for 8 weeks reduced the frequency and severity of attacks compared with placebo, although objective measures of digital blood flow and cold-challenge responses did not change significantly.

    Conclusions

    Evening primrose oil produced symptomatic improvement in Raynaud's attacks without demonstrable change in measured blood flow, a small early trial that has not been convincingly replicated.

    Limitations

    Very small 1980s trial with limited reporting of randomisation and allocation concealment, symptom diaries as primary endpoint, short 8-week duration, and discordance between symptomatic and objective vascular findings.

    Supplements Studied

    Patients receiving EPO benefited symptomatically. This was not matched however by any change in objective assessment of blood flow.

    Related Health Concerns

    Study Details

    Year:1985
    Sample Size:21
    Duration:8 weeks
    Quality Score:5/10

    Disclosures

    Funding

    Industry-supported (Efamol manufacturer)

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