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Evaluation of the Migraceutics® Phase-Specific Dietary Supplement Regimen on Quality of Life, Work Productivity, and Biomarkers in Adult Migraineurs: The Migraceutics® START Study

A Randomized, Sham Supplement- and Care-as-Usual-Controlled Study to Evaluate Migraceutics® Phase-Specific Dietary Supplement Regimen on Quality of Life, Work Productivity, and Biomarkers in Adult Migraineurs: The Migraceutics® START Study

Who can join

As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.

Age
18 Years to 65 Years
Sex
All sexes
Healthy volunteers
Not accepted
Compensation
Not stated

Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.

What to expect

No one can promise a trial will help you personally — that is what the research is trying to find out.

What participation involves

Not stated in the study description — ask the study team about visits and procedures.

Compensation
Not stated
  • Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
  • Participants are monitored closely by the research team throughout the study.
  • Some participants may receive access to an investigational treatment, which is still being studied.
  • Your participation helps researchers learn whether this approach could help future patients.

About this study

In plain language

This study tests a Migraceutics® dietary supplement plan for adults with migraines. It looks at how the plan affects quality of life, work performance, and biomarkers (measurable signs in the body).

The purpose of this study is to evaluate the impact of the Migraceutics® phase-specific dietary supplement regimen on quality of life, work productivity, and biomarkers in adult migraineurs.

Compensation is read from the study's own description and may be missing — always confirm with the study team.

Eligibility

Who can join

  • Report a history of migraines that meets standard migraine diagnosis rules.
  • Be able to take supplements by mouth.
  • Agree to keep your usual lifestyle.
  • Have internet and phone access.

Who can't join

  • Are pregnant or breastfeeding.
  • Have any active health condition other than episodic migraine (migraines that happen from time to time), including liver or kidney problems.
  • Use supplements with overlapping ingredients or medicines that interact with the study supplements.
  • Have a known allergy to any study ingredient.
  • Use alcohol, tobacco, or recreational drugs every day.
  • Take part in another clinical study within 30 days before this study starts or during this study.

Simplified for readability. The official criteria below are what the study team uses.

Official eligibility criteria

Inclusion Criteria: * Self-reported history of migraine, based on the International Headache Society (IHS) International Classification of Headache Disorders, 3rd edition (ICHD-3) diagnostic criteria for migraine. * Being able to take oral supplements. * Agreeing to maintain their regular lifestyle. * Access to internet and telephone. Exclusion Criteria: * Pregnancy or lactation. * Presence of any active medical condition or diagnosis other than episodic migraine, including liver or kidney disease or condition. * Use of overlapping supplements or interacting medications. * Known allergies to study ingredients. * Daily use of alcohol, tobacco, or recreational drugs. * Participation in any other clinical or interventional study within 30 days prior to baseline or concurrently.

Study sites (1)

MD