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NCT04007874RecruitingPhase 4

(WHAT!) – RCT: Open-label randomized controlled trial for the effects of continuous daily use of ethinylestradiol/levonorgestrel (30/150 µg/day) compared with vitamin E (400 IU/day) in the treatment of menstrually-related migraine and perimenopausal migraine

Source: EU CTIS (euclinicaltrials.eu) · Last updated 25 Mar 2026

Brief summary (registry, in English)

To evaluate the effect of continuous daily use of ethinylestradiol/levonorgestrel (30/150 pg/day) compared with vitamin E (400 lU/day) in women: 1. Trial 1: with menstrually-related migraine or pure menstrual migraine; 2. Trial 2: with perimenopausal migraine. The primary efficacy endpoint for the trials is the mean change from baseline in mean monthiy migraine days in a 28-day period as assessed at the 12-week timepoint (weeks 9-12).

Status (registry)
Recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
360 (estimated)
First submitted
11 Oct 2024
Start date
29 Nov 2024
Lead sponsor
Leids Universitair Medisch Centrum (LUMC)
Diseases
Migraine
NCT number
NCT04007874
EU CT number
2024-517127-40-00
EudraCT number
2018-004096-12

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 360
  • 1 site 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, not your situation.

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

  • Smoking - Migraine with aura - Chronic migraine with 15 or more headache days per month/with 8 or more migraine days per month - Medication-overuse headache (ICHD-3 criteria) - Women who are breastfeeding, pregnant, or planning to become pregnant - Oral contraceptive use and not willing to undergo washout period (stop for two consecutive months) - Vitamin E use at start of the study - Use of other sex hormone containing treatments - Increased risk of VTE: history of VTE or thrombophlebitis, hereditary predisposition for VTE (APC resistance, protein C or S deficiency, antithrombin deficiency), VTE in first-degree family member at young age, long term immobilisation - Increased risk of ATE: history of ATE, hereditary predisposition for ATE (hyperhomocysteinemia, antiphospholipid antibodies), ATE in first-degree family member at young age, diabetes mellitus, total cholesterol ≥ 6.5 - Other contraindication for oral contraceptives: liver malignancy, schistosomiasis, HIV/aids, use of immunosuppressives, tuberculosis, sex-hormone-dependent malignancies (breast, endometrial or ovary carcinomas), pancreatitis, vaginal bleeding with unknown cause, other diseases that can influence vessels (malignancies, heart valve disorders, atrial fibrillation, SLE, haemolytic uremic syndrome, chronic inflammatory bowel disease, sickle cell disease) - Contraindication for vitamin E: vitamin K deficiency - Hypersensitivity for any of the compounds in oral contraceptive or vitamin E - Spontaneous postmenopausal status (menstrual bleedings have ceased for 12 consecutive months) - Iatrogenic postmenopausal status - Inability to complete the electronic diary in an accurate manner - Any serious illness that can compromise study participation

Who the study is looking for

  • Trial 1: Menstrually-related migraine: Female - Age ^ 18 - Menstrually-related migraine or pure menstrual migraine - Demonstrated at least 80% compliance with eDiary during baseline period - No or stable for at least two months on prophylactic medication Trial 2: Perimenopausal migraine: Female - AgeS 18 In the early menopausal transition phase (a difference of 7 days or more in length of consecutive cycles, which should occur at least twice in a period of 12 menstrual cycles) - Demonstrated at least 80% compliance with eDiary during baseline period - No or stable for at least two months on prophylactic medication

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

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Leiden University Medical Center
Coordinator of this site? Confirm its status
LeidenNetherlandsRecruiting

Related publications

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