Ketone for Migraine Prevention

NCT05085483 | Completed

• 1 other identifier: 20.08.NRC
• Study Type: interventional
• Target: 54
• Locations: 1 country
• Sites: 1

Brief Summary

Efficacy of a nutritional ketogenic supplement (NKS) in reducing the number, intensity, and duration of migraine headaches in episodic migraine patients.

Conditions

Migraine Headache

Outcome Measures

Primary Outcomes (1)

• Mean change from baseline in MDM versus placebo

  Headache eDiary will be used to record the change in monthly migraine frequency according to ICHD-3 guidelines. The headache diary captures information on date, time of onset and resolution, distinction of migraine from headache based on symptoms, pain intensity and use of acute medication

  1 month

Secondary Outcomes (6)

• Mean change from baseline in the number of headache days of any severity (headache, migraine or probable migraine, and migraine attacks)

  1 month

• Proportion of responders: responders are defined as patients who had a greater than 50%, 75% or 100% reduction in MDM

  1 month

• Reduction in the use of acute medication for migraine

  1 month

• Mean change from baseline in migraine intensity measured with a numerical rating scale from 1 to 10;

  1 month

• Mean change from baseline in the average migraine duration

  1 month

Study Arms (2)

Active intervention (one month)

EXPERIMENTAL

Nutritional Ketogenic Supplement (NKS) 2 x 12 g of EKS/day

Dietary Supplement: Nutritional Ketogenic Supplement

Placebo (one month)

PLACEBO COMPARATOR

Isocaloric placebo supplement

Dietary Supplement: Isocaloric placebo supplement

Interventions

Nutritional Ketogenic Supplement DIETARY_SUPPLEMENT

This trial has 5 steps: (1) a 4-week run-in baseline; (2) a 4-week intervention phase to either active or placebo (3) a 4-week phase of washout; (4) the cross-over to the second 4-week active or placebo phase; (5) a 4-week follow-up.

Active intervention (one month)

Isocaloric placebo supplement DIETARY_SUPPLEMENT

Isocaloric placebo supplement

Placebo (one month)

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Men and women aged ≥18 years who have previously been diagnosed with migraine, with or without aura, in accordance with the ICHD-3 Classification criteria;
• Have an estimated frequency of 5 to 14 MDM in each of the 3 months prior to enrolment;
• In principle, agree at the beginning (virtual call V0) to adequately complete a headache electronic diary (e-Diary) on at least 24 days out of the 28 days in the run-in baseline period;
• In practice, adequately complete by the end of V1 a headache eDiary on at least 24 days out of the 28 days in the run-in baseline period;
• Agree to refrain from initiating or changing the type, dosage, or frequency of any prophylactic medications against migraine, and any treatments for indications other than migraine that in the opinion of the clinician may interfere with the study objectives, e.g. antidepressants, anticonvulsants, beta-blockers, etc. for the duration of the study;
• Women of childbearing potential must agree to use a medically effective form of contraception, unless they can confirm they've had bilateral tubal ligation or that their male partner has had a vasectomy (provided that the partner is the sole sexual partner of the trial participant and that the vasectomised partner has received medical assessment of the surgical success). Medically effective forms of contraception include hormonal methods, such as the contraceptive pill or implant (stable use for at least 3 months prior to enrolment), an intrauterine device (IUD) in use at least 30 days before enrolment, or barrier methods such as diaphragm plus spermicide or condom plus spermicide, in use at least 14 days before enrolment. In circumstances in which hormonal methods may interfere with the action of the IP or placebo, or in which the use of spermicides may increase the risk of transmission of disease, a double-barrier method is recommended.
• Agree to refrain from making any drastic changes to their usual diet for the duration of the study, particularly periods of fasting;
• Have a smartphone with Android or mobile operating system version compatible with eDiary;
• Able to provide informed consent

You may not qualify if:

• Under ketogenic diet, or using exogenous ketone supplements, e.g. medium chain triglycerides (MCT) 1 month prior to the initiation of the study or during the study;
• Patients using regular high dose of Vitamin B3, calcium (\>1 g/day) or magnesium (\>350 mg/day) supplements 1 month prior to the initiation of the study or during the study;
• Suffer from other primary (e.g. tension-type headache, trigeminal autonomic cephalalgias, other primary headache disorders) or secondary headaches (e.g. headaches attributed to trauma or injury, vascular or non-vascular intracranial disorders, substances or their withdrawal, infections, alterations of homeostasis), hemiplegic migraine;
• Pregnancy or intending to become pregnant, or is of childbearing potential and has not had tubal ligation, has a male partner who has not had a successful vasectomy, and is unwilling to use a medically effective form of contraception, i.e. oral contraceptive pills, injectable, or implantable contraceptive; intrauterine device; or double-barrier method (e.g. diaphragm and condom), or is lactating during the study duration. In addition, women of child-bearing potential on hormone-based contraception should not intend to stop or change their contraceptive for the duration of the study;
• Significant medical history, for example diabetes mellitus, renal stones, kidney and liver failure, somatic or psychiatric conditions, uncontrolled hypertension or medicated for hypertension, known hypercalcemia, history of or current cardiovascular disease, chronic gastrointestinal (GI) disease or intestinal malabsorption, or other illness, disease or syndrome which the investigators deem unsuitable to participate in the study;
• Significant medication history, for example use of corticosteroids in format of oral or injectable;
• Vaccination planned 2 weeks prior the start of the study, or during the study;
• Patients following a sodium-restricted diet;
• History of chronic alcohol or substance misuse;
• Previously diagnosed food allergy;
• Is participating in another clinical trial or has participated in a clinical trial the preceding month.

Sponsors & Collaborators

• Société des Produits Nestlé (SPN): lead
• Healint Pte Ltd: collaborator
• Diex Research Sherbrooke Inc.: collaborator

Study Sites (1)

Diex Research Sherbrooke Inc.

Sherbrooke, Quebec, J1L 0H8, Canada

Location

MeSH Terms

Conditions

Migraine Disorders

Condition Hierarchy (Ancestors)

Headache Disorders, Primary; Headache Disorders; Brain Diseases; Central Nervous System Diseases; Nervous System Diseases

Study Officials

• Ginette Girard, MD

  Diex Research Sherbrooke Inc.

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Who Masked: PARTICIPANT, INVESTIGATOR
• Purpose: TREATMENT
• Intervention Model: CROSSOVER
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 18, 2021
• First Posted: October 20, 2021
• Study Start: October 11, 2021
• Primary Completion: November 28, 2022
• Study Completion: November 28, 2022
• Last Updated: March 24, 2023

Record last verified: 2023-03

Data Sharing

• IPD Sharing: Will not share

Locations

CA (1)