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Recruiting NCT05943457

Vitamin K2 Supplementation in Adult Episodic Migraine

No phase Interventional Migraine Headache Arterial Stiffness Vitamin K Deficiency

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Vitamin K2 or menaquinone-7, Placebo.
Who it may be relevant to
Registry conditions: Migraine Headache, Arterial Stiffness, Vitamin K Deficiency. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Lebanon
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Efficacy of Vitamin K2 Supplementation in Adult Episodic Migraine

Overview

Migraine is a debilitating illness and a major cause of disability in the world. It is highly prevalent, especially among women. Vitamin supplementation is a potential therapeutic option for migraines that remains largely under-explored. Several studies have shown that people with migraine tend to have higher arterial stiffness than people without migraine. Vitamin K2 deficiency is an important mediator of arterial stiffness and calcification due to decreased carboxylation of matrix Gla protein (MGP). Supplementation reverses these changes and improves vascular health in patients with end stage renal disease according to previous studies. Therefore, vitamin K2 supplementation could serve a potential role in migraine patients. The purpose of the study is to test the effect of vitamin K2 on decreasing the frequency of migraine attacks and decreasing arterial stiffness. The population will be recruited from the neurology clinic at LAU Medical Center-Rizk Hospital and will constitute of adult patients. They will be randomized to receive either the supplement of vitamin K2 or a placebo for the duration of 6 months. Laboratory tests and arterial stiffness measurements will be done at the beginning, middle, and at the end of the study for comparison.

Interventions

  • Dietary supplement Vitamin K2 or menaquinone-7
    Vitamin K2 (MK7) 360 mcg/day orally once daily for 6 months
  • Other Placebo
    Placebo pills will be administered orally once daily for 6 months

Primary outcome measures

  • Changes of monthly migraine days [Time frame: 6 months]
Secondary outcome measures (6)
  • Changes from baseline in the headache impact score (HIT-6) as compared to placebo. [Time frame: 6 months]
  • Changes from baseline in monthly severe migraine days. [Time frame: 6 months]
  • Changes from baseline on the modified migraine disability assessment (MIDAS) score as compared to placebo. [Time frame: 6 months]
  • Changes from baseline on the modified migraine physical function impact diary (MPFID) as compared to placebo. [Time frame: 6 months]
  • Changes from baseline on the quality of life as measure by the EuroQoL compared to placebo. [Time frame: 6 months]
  • Changes from baseline of arterial stiffness level. [Time frame: 6 months]

Eligibility criteria

Inclusion criteria

  • Adults aged 18 years or above
  • History of episodic migraine with or without aura since > 12 months according to the ICHD-3 criteria.
  • Migraine frequency from 4-14 days per month over the 3 months prior to screening.
  • Migraine frequency from 4-14 days per month during the baseline period of assessment.
  • Successful completion of the migraine diary during the baseline evaluation period.

Exclusion criteria

  • Migraine patients with superimposed tension type or other forms of primary headaches
  • Patients who are currently on any of the migraine prophylactic treatments (Sodium valproate, Topiramate, Beta-blockers, Tricyclic antidepressants, SRNI, Flunarizine, Verapamil, Lisinopril, Candesartan)
  • Patients who have been on any of the previously listed medications within 3 months of screening
  • Patient who takes the following medications:
  • Ergotamine or Triptans > 10 days per month
  • NSAIDs or paracetamol > 15 days per month
  • Opioids more than 4 days per month
  • Patients on anticoagulants
  • Other active chronic pain syndromes (i.e. fibromyalgia, painful peripheral neuropathy, post-herpetic neuralgia…)
  • History of hypersensitivity to the vitamin K2
  • History of soy protein, cheese, eggs and meat allergy
  • History of thrombotic events
  • Diagnosed coagulopathy or any condition related to coagulation
  • Cardiovascular event in the past month
  • Current or planned pregnancy
  • Lactation
  • Inability to tolerate oral medications
  • Known intestinal malabsorption or hypomotility syndromes
  • Atrial fibrillation
  • Active malignancy
  • Any acute illness in the past month

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Quadruple blind
Primary purpose
Treatment

Study locations

Lebanon · 1 center
  • Lebanese American University Medical Center - Rizk Hospital — Beirut

Publications

  • Stovner Lj, Hagen K, Jensen R, Katsarava Z, Lipton R, Scher A, Steiner T, Zwart JA. The global burden of headache: a documentation of headache prevalence and disability worldwide. Cephalalgia. 2007 Mar;27(3):193-210. doi: 10.1111/j.1468-2982.2007.01288.x. PMID 17381554
  • Kurth T, Winter AC, Eliassen AH, Dushkes R, Mukamal KJ, Rimm EB, Willett WC, Manson JE, Rexrode KM. Migraine and risk of cardiovascular disease in women: prospective cohort study. BMJ. 2016 May 31;353:i2610. doi: 10.1136/bmj.i2610. PMID 27247281
  • Mozos I, Stoian D, Luca CT. Crosstalk between Vitamins A, B12, D, K, C, and E Status and Arterial Stiffness. Dis Markers. 2017;2017:8784971. doi: 10.1155/2017/8784971. Epub 2017 Jan 12. PMID 28167849
  • Westenfeld R, Krueger T, Schlieper G, Cranenburg EC, Magdeleyns EJ, Heidenreich S, Holzmann S, Vermeer C, Jahnen-Dechent W, Ketteler M, Floege J, Schurgers LJ. Effect of vitamin K2 supplementation on functional vitamin K deficiency in hemodialysis patients: a randomized trial. Am J Kidney Dis. 2012 Feb;59(2):186-95. doi: 10.1053/j.ajkd.2011.10.041. Epub 2011 Dec 9. PMID 22169620
  • Mansour AG, Hariri E, Daaboul Y, Korjian S, El Alam A, Protogerou AD, Kilany H, Karam A, Stephan A, Bahous SA. Vitamin K2 supplementation and arterial stiffness among renal transplant recipients-a single-arm, single-center clinical trial. J Am Soc Hypertens. 2017 Sep;11(9):589-597. doi: 10.1016/j.jash.2017.07.001. Epub 2017 Jul 13. PMID 28756183
  • Mansour AG, Ahdab R, Daaboul Y, Korjian S, Morrison DA, Hariri E, Salem M, El Khoury C, Riachi N, Aoun Bahous S. Vitamin K2 Status and Arterial Stiffness Among Untreated Migraine Patients: A Case-Control Study. Headache. 2020 Mar;60(3):589-599. doi: 10.1111/head.13715. Epub 2019 Nov 25. PMID 31769041

Identifiers

NCT: NCT05943457 · MK7-003

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗