Migraine Trial, Recruiting NCT04715685 Sponsor: Children's Hospital Medical Center, Cincinnati Condition: Migraine
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Migraine Trial, Recruiting

NCT04715685
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You have been diagnosed with migraine (with or without aura) or chronic migraine that meets standard medical diagnostic guidelines.
  • Over a 28-day headache diary, you have between 4 and 28 headache days per month.
  • Your migraine-related disability score (called PedMIDAS) is above 4 but below 140, meaning migraines cause at least some disruption to daily life but are not at the most extreme level of disability.
  • You are currently taking, or will be on a stable dose throughout the 12-week study of, one or more of these medications or supplements: Vitamin B2, Co-Q10, Magnesium, Vitamin D2 or D3, Depakote, Inderal, Elavil, Topamax, or Periactin.
  • You are able to speak English and complete interviews and questionnaires in English.

Who may not be able to join:

  • You have had a continuous, non-stop headache for an entire 28-day period.
  • You are unable or unwilling to limit use of general pain relievers (such as ibuprofen) to no more than 3 times per week, or migraine-specific medications (such as triptans) to no more than 6 times per month.
  • Your PedMIDAS disability score is above 140, suggesting an extreme level of migraine-related disability.
  • You are pregnant, or sexually active without using an accepted form of contraception such as barrier or hormonal methods.
  • You have a serious psychiatric condition, alcohol or drug dependence, a documented developmental condition (such as autism or cerebral palsy), or any other circumstance that the trial team believes could interfere with safe participation or following the study requirements (confirm with trial site).

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 21 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Scott Powers, PhD, Children's Hospital Medical Center, Cincinnati

Phone: 513-636-9739

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
9 March 2021
Est. completion
1 November 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Change in number of headache days

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov