PArtial REbreathing for Migraine With Aura 1

Stopped early · Not applicable · Has a placebo group

Conditions studied: Migraine With Aura

In brief

A prospective, multi-centre, randomized, double-blind, sham-controlled, parallel-group, group-sequential study to investigate safety and effectiveness of the Rehaler partial rebreathing device, in adults suffering from migraine with aura

Key facts

Study ID

NCT05546385

Run by

Rehaler

People needed

142

Starts

2023-08-08

Expected to finish

2024-10-30

Last updated by the study team

2025-03-25

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Participant has migraine with typical aura (ICHD3 classification 1.2.1) with the additional criterion that historically in more than 75% of cases of aura a moderate or severe headache begins between 10 and 60 minutes after aura onset.
• Participant has had 3 or more migraine-with-aura attacks over the last six months.
• Participant is 18 to 65 years of age.
• Participant's age at onset of migraine with aura was less than 50 years.
• If participant is taking migraine prophylactic drugs, the dose must have been stable for three months or more.
• Participant agrees to withhold usual acute migraine medications until at least two hours after treatment with the study device.
• Participant does not plan to initiate new (and/or change existing) migraine prophylaxis medication for the duration of Stage 1 of the study.
• For female participants: is willing to use adequate contraception during study participation
• Participant owns a smartphone compatible with the ePRO study diary app.
• Participant agrees to use the study device as intended, comply with all study requirements including treatment, follow-up visits, and recording required study data in the ePRO app.
• Participant is willing and able to provide written informed consent.

You may not qualify if…

• Participant has a history of chronic pulmonary disease (e.g. Chronic Obstructive Pulmonary Disease (COPD) or pulmonary fibrosis).
• Participant has a history of severe cardiovascular disease (e.g. symptomatic coronary artery disease, prior myocardial infarction, congestive heart failure) or cerebrovascular disease (e.g. prior stroke or transient ischemic attack, symptomatic carotid artery disease, prior carotid endarterectomy or other vascular neck surgery).
• Participant has a history of intracranial hyper/hypo-tension.
• Participant has a history of cerebral aneurysm.
• Participant has had previous brain surgery, including stenting.
• Anaemia, defined as a hemoglobin concentration in capillary blood lower than 11g/dL
• Participant has a baseline SPO2 level which is lower than 95% performed at Site Visit 1.
• Participant has 15 or more headache days per month
• Participant has medication-overuse headache (ICHD3 classification 8.2).
• Participant has a known history or suspicion of recurring secondary headache which in the opinion of the investigator may interfere with the study.
• Hemiplegic migraine
• Participant has other significant and relevant pain problem (e.g. cancer pain, fibromyalgia or other head or facial pain disorders)
• Participant has a known history or suspicion of substance abuse or addiction (within the last 5 years) that in the opinion of the investigator may confound the study assessments.
• Participant has a history of psychiatric or cognitive disorder and/or behavioural problems which in the opinion of the investigator may interfere with the study.
• Participant belongs to a vulnerable population or has any condition such that his or her ability to provide informed consent, comply with the follow-up requirements, or provide self-assessments is compromised (e.g. homeless, developmentally disabled, prisoner).
• For female participants: is pregnant or actively trying to become pregnant.
• Participant is participating in any other clinical investigation or has participated in an interventional clinical trial in the preceding 30 days.
• Participant has any condition that according to the investigator may pose the participant at risk or provide confounding data.
• Participant is unable, as perceived by study personnel, to correctly understand and follow the instructions for use of the device and ePRO app.
• Sickle Cell Disease
• Participant is being treated with nerve blocks or injections for migraine prophylaxis on a regularly scheduled basis (including Botox, Aimovig/Erenumab, Ajovy/Fremanezumab, Emgality/Galcanezumab or Vyepti/Eptinezumab).

Where it is running

• Stanford University - Stanford Headache Clinic — Palo Alto, California, United States
• Profound Research-Southern California Neurology Consultants — Pasadena, California, United States
• Artemis Institute for Clinical Research — Riverside, California, United States
• Yale University — New Haven, Connecticut, United States
• MedStar Health Research Institute — Washington D.C., District of Columbia, United States
• University of Miami — Miami, Florida, United States
• PharmaSite Research — Baltimore, Maryland, United States
• Clinvest Research — Springfield, Missouri, United States
• Thomas Jefferson University Hospital — Philadelphia, Pennsylvania, United States
• Charité University Hospital — Berlin, Germany
• Essen University Hospital-West German Headache Center — Essen, Germany
• Frankfurt Headache Center — Frankfurt, Germany
• University Hospital Freiburg — Freiburg im Breisgau, Germany
• Jena University Hospital — Jena, Germany
• Munich University Hospital — Munich, Germany

Full record on ClinicalTrials.gov

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