Vitamin K2 Supplementation in Adult Episodic Migraine (ViKEM)

Sola Aoun Bahous, M.D. Ph.D.

Status: Not yet enrolling

Conditions: Vitamin K Deficiency; Migraine Headache; Arterial Stiffness

Treatments: Other: Placebo; Dietary Supplement: Vitamin K2 or menaquinone-7

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT05943457

MK7-003

Details and patient eligibility

About

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.

Enrollment: 160 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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160 participants in 2 patient groups, including a placebo group

Intervention (MK7) Arm

Experimental group

Description:

This corresponds to the sub-group of subjects who will receive the supplement (vitamin K2 or Menaquinone-7).

Treatment:

Dietary Supplement: Vitamin K2 or menaquinone-7

Control Arm

Placebo Comparator group

Description:

This corresponds to the sub-group of subjects who will receive placebo.

Treatment:

Other: Placebo