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Tanacetum parthenium

Feverfew

Research reviewed: Up until 03/2026

Feverfew (Tanacetum parthenium) is a dietary supplement with 5 published peer-reviewed studies involving 899 participants, researched for Migraine Prevention, Anti-Inflammatory & Pain Relief.

5
Studies
899
Participants
2000–2025
Research Span

Evidence at a Glance

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

Overall: Moderate Evidence

Migraine Prevention

Moderate
3 studies 2 of 3 positive 625 participants

Anti-Inflammatory & Pain Relief

Weak
2 studies 0 of 2 positive 245 participants

Research Visualised

Visual breakdown of the clinical data.

Study Quality Breakdown

What types of studies were conducted

3/5
Randomised
3/5
Double-Blind
3/5
Placebo-Controlled

Participants Per Study

Larger samples = more reliable results

Study 1 (2025)
9
Study 2 (2015)
561
Study 3 (2004)
55
Study 1 (2005)
0
Study 2 (2000)
245

Research Timeline

When the studies were published

1
2000
1
2004
1
2005
1
2015
1
2025

All Studies

Detailed breakdown of each trial. Click to expand.

Migraine Prevention

1

To evaluate the efficacy of Tanacetum parthenium (feverfew) in migraine relief

2025 9 participants Various (8-16 weeks typical) Various feverfew preparations (50-150 mg/day typical)
Human Study Positive

Study Type

Systematic review and meta-analysis

Purpose

To evaluate the efficacy of Tanacetum parthenium (feverfew) in migraine relief

Dose

Various feverfew preparations (50-150 mg/day typical)

Participants

Meta-analysis of 9 double-masked, placebo-controlled RCTs (899 participants)

Duration

Various (8-16 weeks typical)

Results

Feverfew significantly reduced migraine attack frequency and migraine duration. Showed non-significant trend toward reduced pain severity.

How They Measured It

Migraine frequency, duration, pain severity

Read full study
2

To assess evidence for feverfew in preventing migraine

2015 561 participants Various Various feverfew doses and preparations
Human Study Mixed

Study Type

Cochrane systematic review

Purpose

To assess evidence for feverfew in preventing migraine

Dose

Various feverfew doses and preparations

Participants

561 patients with migraine history

Duration

Various

Results

One larger, rigorous study showed feverfew reduced migraine frequency by 0.6 per month compared to placebo. However, no effect on pain severity or duration.

How They Measured It

Meta-analysis of 6 RCTs on migraine frequency

Read full study
3

To evaluate combination treatment of riboflavin, magnesium, and feverfew for migraine prophylaxis

2004 55 participants 3 months 2.65 mg feverfew in combination
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomized, double-blind, placebo-controlled

Purpose

To evaluate combination treatment of riboflavin, magnesium, and feverfew for migraine prophylaxis

Dose

2.65 mg feverfew in combination

Participants

55 patients with frequent migraines

Duration

3 months

Results

Combination including feverfew showed significant reduction in migraine frequency compared to placebo.

How They Measured It

Migraine frequency and severity

Read full study

Anti-Inflammatory & Pain Relief

1

To evaluate the safety and efficacy of 6.25 mg feverfew CO2-extract (MIG-99) in migraine prevention

2005 ? participants 12 weeks MIG-99 6.25 mg t.i.d.
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomized, double-blind, placebo-controlled

Purpose

To evaluate the safety and efficacy of 6.25 mg feverfew CO2-extract (MIG-99) in migraine prevention

Dose

MIG-99 6.25 mg t.i.d.

Participants

Adult migraine patients

Duration

12 weeks

Results

Although some improvement noted, MIG-99 6.25 mg t.i.d. failed to show significant migraine prophylactic effect compared to placebo in this particular study.

How They Measured It

Migraine frequency, pain intensity

Read full study
2

To evaluate the efficacy and safety of standardized Tanacetum parthenium for migraine prophylaxis with dose-response analysis

2000 245 participants 12 weeks 0.3 mg, 1 mg, and 2.7 mg parthenolide (active component)
Human Study RCT Double-Blind Placebo Mixed

Study Type

Randomized, double-blind, placebo-controlled

Purpose

To evaluate the efficacy and safety of standardized Tanacetum parthenium for migraine prophylaxis with dose-response analysis

Dose

0.3 mg, 1 mg, and 2.7 mg parthenolide (active component)

Participants

245 patients with migraine history

Duration

12 weeks

Results

Dose-response analysis of feverfew showed efficacy for migraine prevention with optimal effects at higher standardized doses.

How They Measured It

Migraine frequency, severity, associated symptoms

Read full study

Frequently Asked Questions

Common questions about Feverfew research

What does the research say about Feverfew?

There are currently 10 peer-reviewed studies on Feverfew (Tanacetum parthenium), involving 899 total participants. Research covers Migraine prevention, Anti-inflammatory, Pain relief. The overall evidence strength is rated as Moderate.

How strong is the evidence for Feverfew?

The evidence is currently rated as "Moderate Evidence". This rating is based on study design quality (randomisation, blinding, placebo controls), sample sizes, study types (5 human studies), and reported outcomes.

What health goals has Feverfew been studied for?

Feverfew has been researched for: Migraine prevention, Anti-inflammatory, Pain relief. Each area has its own body of evidence which you can explore in the study breakdowns above.

Are the studies on Feverfew based on human trials?

Yes, 5 out of 10 studies are human trials. Human trials carry more weight in our evidence scoring system.