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A multicentre, triple blind, placebo controlled, parallel group study of atorvastatin in episodic migraine (StatinMigEpisodic)

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2022-502176-23-01
Acronym
StatinMigEpisodic
Enrollment
450
Registered
2023-06-23
Start date
2024-05-13
Completion date
Unknown
Last updated
2024-06-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Migraine

Brief summary

Difference between groups receiving atorvastatin 40 mg daily and placebo in change from baseline in number of migraine days per 4 weeks

Detailed description

Difference between groups receiving atorvastatin 40 mg daily and placebo in change from baseline in number of headache per 4 weeks, Difference in change from baseline between groups receiving atorvastatin 20 mg daily and placebo in number of days with headache per 4 weeks,, Number of responders (≥ 50% decrease in migraine days compared with baseline) between repectively Atorvastin 40 mg, Atorvastatin 20 mg and placebo

Interventions

DRUGATORVASTATIN
DRUGPLACEBO

Sponsors

St. Olavs Hospital HF, St. Olavs Hospital HF
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Design outcomes

Primary

MeasureTime frame
Difference between groups receiving atorvastatin 40 mg daily and placebo in change from baseline in number of migraine days per 4 weeks

Secondary

MeasureTime frame
Difference between groups receiving atorvastatin 40 mg daily and placebo in change from baseline in number of headache per 4 weeks, Difference in change from baseline between groups receiving atorvastatin 20 mg daily and placebo in number of days with headache per 4 weeks,, Number of responders (≥ 50% decrease in migraine days compared with baseline) between repectively Atorvastin 40 mg, Atorvastatin 20 mg and placebo

Countries

Norway

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026