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2022-502176-23-01RecruitingPhase 2

Atorvastatin in episodic migraine

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

Source: EU CTIS (euclinicaltrials.eu) · Last updated 14 Apr 2026

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Brief summary (registry, in English)

To evaluate whether the favourable preventative effect ofAtorvastin in two different doses seen in three smaller studies, can be confirmed in a larger multicentre randomized, controlled study

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
450 (estimated)
First submitted
22 Mar 2023
Start date
13 May 2024
Lead sponsor
St. Olavs Hospital HF
Diseases
Migraine
EU CT number
2022-502176-23-01

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 450
  • 5 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Interval headache not distinguishable from migraine or chronic migraine, chronic tension-type headache, medication overuse headache or other headache occurring on ≥ 15 days/month.
  • Hypersensitivity to statins or previous use of statins
  • Use of medicines for migraine prophylaxis less than 4 weeks, or of botulinum toxin less than 16 weeks, prior to start of study
  • Having tried ≥ 3 prophylactic drugs against migraine during the last 10 years
  • Consistently failing to respond to any acute migraine medication and/or requiring detoxification from acute medication (triptans, opioids)

Other illness

  • Clinical information on signs of cholestasis, decreased hepatic or renal function, high degree of comorbidity, frailty associated with reduced life expectancy, high likelihood of hospitalization at the discretion of the investigator,, history of angioneurotic oedema, current use of antiviral treatment against hepatitis C, significant psychiatric illness, alcohol or illicit drug dependence, inability to understand study procedures and to comply with them for the entire length of the study, and/or treatment for hypothyroidism

Other

  • Pregnancy, planning to get pregnant, inability to use contraceptives or lactating.

Who the study is looking for

  • Aged 18 to 65 years with 4-14 migraine days per month
  • Signed informed consent
  • Episodic migraine with or without aura according to ICHD-3 criteria, debut of migraine at least one year prior to inclusion, and start of migraine before age 50 years
  • No use of other migraine prophylactics during the study
  • For women of child-bearing potential there must be no pregnancy or planned pregnancy during the study period, and use of highly effective contraception

Age in the registry: 18 years to 64 years · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (5)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Helse Bergen HFBergenNorwayRecruiting
Akershus University HospitalLørenskogNorwayRecruiting
Oslo University Hospital HFOsloNorwayRecruiting
Universitetssykehuset Nord-NorgeTromsøNorwayRecruiting
St. Olavs hospital HFTrondheimNorwayRecruiting

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This page is information, not medical advice. Discuss any trial with your doctor.