Migraine Trial, Recruiting NCT05889624 Sponsor: Children's Hospital Medical Center, Cincinnati Condition: Migraine
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Migraine Trial, Recruiting

NCT05889624
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:

  • People who have been diagnosed with migraine (with or without aura) according to standard headache disorder guidelines, or who have ongoing headaches that include migraine episodes — including those who may be overusing pain medications
  • People who have had 4 or more headache days in a 28-day period, tracked using a headache diary before joining the trial
  • People whose doctor at the trial site has determined that a medication called amitriptyline would be a suitable preventive treatment for their migraines
  • People who are able to complete study visits and questionnaires in English

Who may not be able to join:

  • People who are currently using amitriptyline, or are currently receiving a type of talking therapy called Cognitive Behavioural Therapy (CBT) specifically for headache treatment
  • People who are currently taking another prescribed medication to prevent migraines, if it has been taken within a certain recent time period related to how long that medication stays in the body (confirm with trial site)
  • People who are currently receiving Botox injections or a type of medication called CGRP monoclonal antibodies for migraine prevention
  • Young people who are currently pregnant
  • People who are currently experiencing suicidal thoughts, or who have made a suicide attempt in the past six months, or who have a history of bipolar disorder, a heart condition called prolonged QT, or significant ongoing constipation or slow stomach emptying
  • People who have any other health condition that, in the trial doctor's opinion, would make them unsuitable for the study or could interfere with their medical care

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 26 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, Cincinnati Childrens 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
22 August 2023
Est. completion
31 July 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Change in number of headache days; Reduction to a PedMIDAS score of 20 or less

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: 26 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