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
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Disclosures
Funding
Industry-supported (Efamol manufacturer)
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