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Oenothera biennis seed oil

Evening Primrose Oil

Research reviewed: Up until 03/2026

Evening Primrose Oil (Oenothera biennis seed oil) is a dietary supplement with 8 published peer-reviewed studies involving 1,680 participants, researched for Skin Health, PMS & Menopause, Breast Pain and 1 more areas.

8
Studies
1,680
Participants
1988–2013
Research Span

Evidence at a Glance

Strength is scored by study design, sample size, study type, and outcomes

Overall: Very Strong Evidence

Skin Health

Moderate
2 studies 1 of 2 positive 108 participants

PMS & Menopause

Strong
2 studies 2 of 2 positive 176 participants

Breast Pain

Moderate
1 study 1 of 1 positive 200 participants

Rheumatoid Arthritis

Moderate
3 studies 2 of 3 positive 94 participants 2 human

Research Visualised

Visual breakdown of the clinical data.

Study Quality Breakdown

What types of studies were conducted

5/8
Randomised
5/8
Double-Blind
5/8
Placebo-Controlled

Participants Per Study

Larger samples = more reliable results

Study 1 (1995)
99
Study 2 (2003)
9
Study 1 (2010)
120
Study 2 (2013)
56
Study 1 (2000)
200
Study 1 (1988)
94
Study 2 (2002)
0
Study 3 (2005)
0

Research Timeline

When the studies were published

1
1988
1
1995
1
2000
1
2002
1
2003
1
2005
1
2010
1
2013

All Studies

Detailed breakdown of each trial. Click to expand.

Skin Health

1

To evaluate evening primrose oil (EPO) for atopic eczema.

1995 99 participants 20 weeks 500 mg/day EPO (6% GLA)
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To evaluate evening primrose oil (EPO) for atopic eczema.

Dose

500 mg/day EPO (6% GLA)

Participants

99 patients with atopic eczema

Duration

20 weeks

Results

EPO significantly improved overall eczema severity, reducing itch, redness, and scaling compared to placebo. Red blood cell GLA levels increased proportionally to improvement in skin symptoms.

How They Measured It

Overall severity score, itch, redness, scaling

Read full study
2

To evaluate EPO supplementation for atopic eczema.

2003 9 participants Various Various EPO doses
Human Study Positive

Study Type

Meta-analysis

Purpose

To evaluate EPO supplementation for atopic eczema.

Dose

Various EPO doses

Participants

Pooled from 9 controlled trials (>700 patients)

Duration

Various

Results

EPO showed significant overall improvement in atopic eczema in meta-analysis. Subgroup analyses showed particularly strong effects on itch and skin inflammation. Quality of evidence varies across trials.

How They Measured It

Pooled symptom severity across RCTs

Read full study

PMS & Menopause

1

To evaluate EPO on premenstrual syndrome symptoms.

2010 120 participants 6 months 3 g/day EPO
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To evaluate EPO on premenstrual syndrome symptoms.

Dose

3 g/day EPO

Participants

120 women with PMS

Duration

6 months

Results

EPO significantly reduced breast pain, mood disturbances, and water retention in PMS. The effect was attributed to GLA-derived prostaglandin E1 which modulates hormonal responses.

How They Measured It

PMS symptom diary, pain VAS, psychological symptoms

Read full study
2

To assess EPO supplementation on hot flushes in menopausal women.

2013 56 participants 6 weeks 500 mg EPO twice daily
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To assess EPO supplementation on hot flushes in menopausal women.

Dose

500 mg EPO twice daily

Participants

56 postmenopausal women with hot flushes

Duration

6 weeks

Results

EPO significantly reduced hot flush frequency and severity compared to placebo. Kupperman Index scores improved. EPO appears to reduce the intensity rather than frequency of menopausal flushing.

How They Measured It

Hot flush frequency and severity (diary), Kupperman Index

Read full study

Breast Pain

1

To evaluate EPO for mastalgia (breast pain) in premenopausal women.

2000 200 participants 6 months 3 g/day EPO
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To evaluate EPO for mastalgia (breast pain) in premenopausal women.

Dose

3 g/day EPO

Participants

200 women with cyclical mastalgia

Duration

6 months

Results

EPO significantly reduced cyclical breast pain severity compared to placebo. Approximately 45% of EPO-treated women experienced significant symptom relief. The response rate was lower for non-cyclical mastalgia.

How They Measured It

Cardiff Breast Pain chart, pain VAS, breast tenderness score

Read full study

Rheumatoid Arthritis

1

To assess EPO supplementation on symptoms and medication use in rheumatoid arthritis.

1988 94 participants 12 months 6 g/day EPO (540 mg/day GLA)
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To assess EPO supplementation on symptoms and medication use in rheumatoid arthritis.

Dose

6 g/day EPO (540 mg/day GLA)

Participants

94 patients with rheumatoid arthritis

Duration

12 months

Results

EPO significantly reduced morning stiffness and joint tenderness. NSAID use was significantly reduced in the EPO group. The anti-inflammatory mechanism is via GLA-derived dihomo-GLA.

How They Measured It

Morning stiffness duration, joint tenderness, NSAID use

Read full study
2

To evaluate EPO and other GLA sources for rheumatoid arthritis.

2002 ? participants Various Various
Human Study Mixed

Study Type

Systematic review

Purpose

To evaluate EPO and other GLA sources for rheumatoid arthritis.

Dose

Various

Participants

Multiple RCT populations

Duration

Various

Results

EPO and borage oil (high GLA) supplementation consistently reduced joint tenderness and morning stiffness in RA. Higher GLA content sources showed greater effects. Well tolerated compared to standard disease-modifying drugs.

How They Measured It

Review of RCTs on joint symptoms, medication use, disease activity scores

Read full study
3

To investigate EPO on prostaglandin profiles and joint inflammation in adjuvant-induced arthritis.

2005 ? participants 21 days 1 mL/kg/day EPO
Animal Study Positive

Study Type

Animal study

Purpose

To investigate EPO on prostaglandin profiles and joint inflammation in adjuvant-induced arthritis.

Dose

1 mL/kg/day EPO

Participants

Sprague-Dawley rats

Duration

21 days

Results

EPO supplementation significantly reduced joint swelling and shifted prostaglandin profiles from pro-inflammatory PGE2 to anti-inflammatory PGE1. Paw oedema was reduced by 62% compared to control.

How They Measured It

Joint swelling, PGE2 and PGE1 levels, paw weight

Read full study

Frequently Asked Questions

Common questions about Evening Primrose Oil research

What does the research say about Evening Primrose Oil?

There are currently 10 peer-reviewed studies on Evening Primrose Oil (Oenothera biennis seed oil), involving 1,680 total participants. Research covers Skin health (eczema), PMS & menopause, Breast pain and 1 more areas. The overall evidence strength is rated as Very Strong.

How strong is the evidence for Evening Primrose Oil?

The evidence is currently rated as "Very Strong Evidence". This rating is based on study design quality (randomisation, blinding, placebo controls), sample sizes, study types (7 human studies, 1 animal study), and reported outcomes.

What health goals has Evening Primrose Oil been studied for?

Evening Primrose Oil has been researched for: Skin health (eczema), PMS & menopause, Breast pain, Rheumatoid arthritis. Each area has its own body of evidence which you can explore in the study breakdowns above.

Are the studies on Evening Primrose Oil based on human trials?

Yes, 7 out of 10 studies are human trials. The remaining 1 is an animal study. Human trials carry more weight in our evidence scoring system.