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Migraine Headaches Elimination With Patent Foramen Ovale-Directed Therapy (COMFORT-PFO)

2026. július 28. frissítette: Robert Sommer, Columbia University

Cessation of Migraine Headaches With Patent Foramen Ovale-Directed Therapy (COMFORT - PFO): An Investigator-Initiated Study

Migraine is a common and often disabling condition, but its exact causes are not fully understood. Some people with migraines have a small opening in the heart wall called a patent foramen ovale (PFO). In some of these patients, closing this opening or taking a medication that inhibits blood platelets (prasugrel) has been shown to reduce migraines. However, not everyone benefits, and it is unclear why. This study is being done to better understand whether closing a PFO can provide lasting migraine relief - especially in patients whose migraines improve with prasugrel.

The goal of this study is to find out whether, in patients whose migraines improve while taking prasugrel, closing the PFO along with 24 weeks of prasugrel leads to better long-term migraine relief after stopping the medication, than by taking prasugrel for 24 weeks alone.

Participants will track their migraines daily using an electronic diary, then take prasugrel and compare their migraines while on the medication. Only patients whose migraines improve on this medication will continue in the study. Eligible participants will be randomly assigned (like flipping a coin) to one of two groups: 1) Medication-only group: Continue prasugrel for 24 weeks. 2) Procedure group: Undergo a minimally invasive procedure to close the PFO and continue prasugrel for 24 weeks. After treatment, the medication will be stopped in both groups, and participants will again track their migraines for about 8 weeks.

The main question is: Do patients who have PFO closure continue to have fewer migraines after stopping prasugrel compared with those who did not have the procedure?

A tanulmány áttekintése

Részletes leírás

The hypothesis of the COMFORT-PFO Study is that a subset of migraine patients with PFO have an underlying platelet-mediated migraine mechanism in which byproducts of platelet activation or aggregation enter the cerebral circulation via the PFO at supraphysiologic levels, thereby triggering migraine.

Inhibition of platelet activity with thienopyridine therapy is expected to reduce the generation of these byproducts in the systemic venous circulation and, consequently, their passage to the cerebral circulation. Similarly, transcatheter closure of the PFO eliminates the right-to-left pathway, resulting in reduced exposure of the brain to these platelet-derived factors. In this context, a response to thienopyridine therapy may serve as a clinical marker to identify patients in whom the PFO plays a mechanistic role in migraine pathophysiology.

The primary objective of this study is to evaluate whether the clinical benefit in migraine reduction observed during initial thienopyridine therapy is maintained after treatment withdrawal, comparing subjects assigned to transcatheter PFO closure with those managed with medical therapy alone. Thienopyridine-responsiveness will be assessed using prasugrel hydrochloride in this study.

Tanulmány típusa

Beavatkozó

Beiratkozás (Becsült)

32

Fázis

  • 3. fázis

Kapcsolatok és helyek

Ez a rész a vizsgálatot végzők elérhetőségeit, valamint a vizsgálat lefolytatásának helyére vonatkozó információkat tartalmazza.

Tanulmányi kapcsolat

Tanulmányozza a kapcsolattartók biztonsági mentését

Tanulmányi helyek

    • New York
      • New York, New York, Egyesült Államok, 10032
        • Columbia University Irving Medical Center - NewYork Presbyterian Hospital (CUIMC/NYP)
        • Kapcsolatba lépni:
        • Kapcsolatba lépni:
        • Kutatásvezető:
          • Robert J Sommer, MD

Részvételi kritériumok

A kutatók olyan embereket keresnek, akik megfelelnek egy bizonyos leírásnak, az úgynevezett jogosultsági kritériumoknak. Néhány példa ezekre a kritériumokra a személy általános egészségi állapota vagy a korábbi kezelések.

Jogosultsági kritériumok

Tanulmányozható életkorok

  • Felnőtt

Egészséges önkénteseket fogad

Nem

Leírás

Patient Inclusion Criteria:

  • Age: ≥18 and <55 at time of screening
  • Migraine headache with aura, or migraine headache without aura, fulfilling conditions of the Neurology Screening Tool (meeting ICHD-3 criteria)
  • Diagnosis of migraine for ≥ 1 year; onset of migraine symptoms < 40 years of age
  • By history, an average headache burden of greater than one migraine headache day per week:
  • without current preventative therapy, OR
  • despite preventative therapy, OR
  • with reason to come off effective therapy (e.g. cost, aversion to injections, side effects)
  • If patient is taking preventive migraine medications, dose must be stable for at least 3 months prior to the screening visit. Patient agrees to continue preventive medication at the current dosage throughout the duration of the Baseline and On-treatment monitoring periods (Study Weeks 1 - 17).
  • Female patients capable of becoming pregnant agree to use two forms of birth control or abstinence during their participation in the study.

Patient Exclusion Criteria:

Exclusions due to underlying patient medical issues:

  • Headache disorder other than migraine with aura, or migraine without aura
  • Patient has history of stroke, TIA, or intracranial hemorrhage.
  • Patient has a history of thrombocytopenia within one year, or platelet count <100,000/mm3 identified during the screening laboratory evaluation.
  • Patient has severe hepatic impairment with reduced synthetic function as documented by prolongation of PT/PTT, or with total bilirubin >3.0 mg/dL identified during the screening laboratory evaluation.
  • Patient has previously implanted pacemaker, IVC filter, PFO closure device, ASD closure device, or left atrial appendage closure device or any cardiac history which, in the investigator's opinion, would preclude them from study participation.
  • Patient has documented right-to-left shunt source in addition to PFO such as atrial septal defect or pulmonary arteriovenous malformation.
  • Patient has a history of clinically significant bleeding within 6 months of the screening visit, any active bleeding, or active peptic ulcer disease.
  • Patient has an uncontrolled arrhythmia, or if on therapy, has evidence of arrhythmia control failure within the past 90 days (e.g., supraventricular tachycardia or atrial fibrillation while under rhythm control).
  • Patient has elevated PVR which in the opinion of the implanting physician precludes safe PFO closure.
  • Patient has active infection at the time of screening that cannot be treated.
  • Patient is planning surgery during the study timeframe.
  • A female patient is pregnant or is planning pregnancy during the anticipated duration of the study. Urine or blood pregnancy screening will be performed as part of the screening laboratory evaluation.
  • Patient has documented nickel allergy/sensitivity
  • Patient has a documented history of non-compliance with medical care, which would preclude them, in the opinion of the study team

Exclusion Due to Medication Restrictions:

  • Patient has known hypersensitivity or contraindication to thienopyridines
  • Patient has another medical condition requiring chronic antithrombotic therapy with antiplatelet, oral anticoagulant or injectable agents
  • Patient has need for daily use of NSAIDs other than for treatment of migraines

Tanulási terv

Ez a rész a vizsgálati terv részleteit tartalmazza, beleértve a vizsgálat megtervezését és a vizsgálat mérését.

Hogyan készül a tanulmány?

Tervezési részletek

  • Elsődleges cél: Megelőzés
  • Kiosztás: Véletlenszerűsített
  • Beavatkozó modell: Párhuzamos hozzárendelés
  • Maszkolás: Nincs (Open Label)

Fegyverek és beavatkozások

Résztvevő csoport / kar
Beavatkozás / kezelés
Aktív összehasonlító: Group A - Thienopyridine only
16 patients will be randomized to this group. Thienopyridine medication (prasugrel) which was demonstrated to reduce headache frequency during study screening phases, will be continued for 6 months and then stopped. Post-therapy headache frequency will be compared with the patient's baseline headache frequency. After completion of the study procedures, patients in this group will be given the opportunity to get the PFO closure procedure.
Six months of daily prasugrel therapy following randomization.
Más nevek:
  • Prasugrel Hydrochloride
Aktív összehasonlító: Group B - PFO closure plus thienopyridine
16 patients will be randomized to this group. After demonstrating thienopyridine (prasugrel) benefit for migraine symptoms in the screening phases of the study, patients in this arm will undergo PFO closure, a non-surgical outpatient catheter procedure. They will remain on prasugrel for an additional 6 months. The medication will then be stopped. Post-therapy headache frequency will be compared with the patient's baseline headache frequency.
Six months of daily prasugrel therapy following randomization.
Más nevek:
  • Prasugrel Hydrochloride
A standard transcatheter closure of PFO will be performed in the Group B cohort. During this non-surgical procedure, the GORE Cardioform Septal Occluder will be used to close the PFO (it is FDA-approved for exactly this purpose for prevention of recurrent stroke) but will be used here in an off-label fashion.

Mit mér a tanulmány?

Elsődleges eredményintézkedések

Eredménymérő
Intézkedés leírása
Időkeret
Reduction in Monthly Migraine Days (MMD)
Időkeret: upon completion of the 56-day Post-Therapy monitoring session
The primary efficacy endpoint is the proportion of randomized subjects maintaining a clinically meaningful migraine response, defined as a ≥50% reduction in Monthly Migraine Days (MMD) in the Post-Therapy monitoring session, compared with the Baseline monitoring session (following discontinuation of prasugrel).
upon completion of the 56-day Post-Therapy monitoring session

Másodlagos eredményintézkedések

Eredménymérő
Intézkedés leírása
Időkeret
Effect Persistence (EP)
Időkeret: upon completion of the 56-day Post-Therapy monitoring session

Effect Preservation (EP) is a constructed metric which defines the extent to which the clinical benefit of migraine reduction observed during thienopyridine therapy is maintained following discontinuation of therapy.

EP is calculated for each randomized subject as the proportion of the On-Therapy reduction in Monthly Migraine Days (MMD) that is preserved during the Post-Therapy period, expressed as a percentage.

For each subject, EP is defined as:

EP = (Post-Therapy Reduction in MMD / On-Therapy Reduction in MMD) × 100 where:

Post-Therapy Reduction in MMD = Baseline MMD - Post-Therapy MMD

On-Therapy Reduction in MMD = Baseline MMD - On-Therapy MMD

EP provides a continuous, subject-level measure of treatment durability, allowing comparison of the extent to which the initial treatment effect is maintained following therapy discontinuation.

upon completion of the 56-day Post-Therapy monitoring session
Responder-based Endpoints
Időkeret: upon completion of the 56-day Post-Therapy monitoring session

Responder-based endpoints will assess higher thresholds of clinical response and will include the proportion of subjects achieving:

  • ≥75% reduction in MMD from Baseline during the Post-Therapy monitoring period
  • ≥90% reduction in MMD from Baseline, representing near complete elimination of migraine days
  • 100% reduction in MMD from Baseline, representing complete elimination of migraine days.
upon completion of the 56-day Post-Therapy monitoring session
Absolute reduction in MMD from Baseline to Post-Therapy
Időkeret: upon completion of the 56-day Post-Therapy monitoring session
This measure will calculate the absolute difference in MMD between the Baseline monitoring session and the Post-Therapy monitoring session.
upon completion of the 56-day Post-Therapy monitoring session
Percent reduction in MMD from Baseline to Post-Therapy
Időkeret: upon completion of the 56-day Post-Therapy monitoring session
This measure will assess the percentage difference in MMD between the Baseline monitoring session and the Post-Therapy session.
upon completion of the 56-day Post-Therapy monitoring session
Change in MSQ 2.1 Score (Baseline Score - Post-thienopyridine Score)
Időkeret: Baseline and upon completion of the 56-day Post-Therapy monitoring session
The Migraine-Specific Quality of Life Questionnaire (MSQ) Version 2.1 is a 14-item patient-reported questionnaire to evaluate the impact of migraines on a patient's quality of life across 3 domains: Role Function-Restrictive (measures how migraines limit daily, social, and work-related activities), Role Function-Preventive (measures how migraines prevent these daily activities from happening altogether), and Emotional Function (assesses the emotional toll, frustration, and helplessness caused by migraines). In this modified version, the minimum score is 0, and the maximum score is 70, with each answer to the 14 questions receiving from 0 to 5 points. The cumulative score will be assessed at Baseline and after Treatment. The lower the score, the better Quality of Life. The absolute difference in the cumulative score will be compared, with a reduction from baseline indicating an improvement in quality of life.
Baseline and upon completion of the 56-day Post-Therapy monitoring session
Change in HIT-6 Score (Baseline Score - Post-thienopyridine Score)
Időkeret: Baseline and upon completion of the 56-day Post-Therapy monitoring session
The HIT-6 (Headache Impact Test) is a 6-item patient-reported questionnaire that measures how severely headaches impact daily life, social functioning, and ability to concentrate. Scores range from 36 to 78, with higher numbers indicating greater headache-related disability. This measure will assess the difference from the Baseline (at enrollment) HIT-6 score, to the HIT-6 score after completion of the Post-Therapy monitoring session. A decrease in the HIT-6 score reflects a reduction of the life impact imposed by migraines.
Baseline and upon completion of the 56-day Post-Therapy monitoring session

Együttműködők és nyomozók

Itt találhatja meg a tanulmányban érintett személyeket és szervezeteket.

Nyomozók

  • Kutatásvezető: Robert J Sommer, MD, Columbia University
  • Kutatásvezető: Jessica Ailani, MD, MedStar Georgetown University Hospital

Publikációk és hasznos linkek

A vizsgálattal kapcsolatos információk beviteléért felelős személy önkéntesen bocsátja rendelkezésre ezeket a kiadványokat. Ezek bármiről szólhatnak, ami a tanulmányhoz kapcsolódik.

Általános kiadványok

Tanulmányi rekorddátumok

Ezek a dátumok nyomon követik a ClinicalTrials.gov webhelyre benyújtott vizsgálati rekordok és összefoglaló eredmények benyújtásának folyamatát. A vizsgálati feljegyzéseket és a jelentett eredményeket a Nemzeti Orvostudományi Könyvtár (NLM) felülvizsgálja, hogy megbizonyosodjon arról, hogy megfelelnek-e az adott minőség-ellenőrzési szabványoknak, mielőtt közzéteszik őket a nyilvános weboldalon.

Tanulmány főbb dátumok

Tanulmány kezdete (Becsült)

2026. szeptember 1.

Elsődleges befejezés (Becsült)

2027. december 1.

A tanulmány befejezése (Becsült)

2028. március 1.

Tanulmányi regisztráció dátumai

Először benyújtva

2026. május 22.

Először nyújtották be, amely megfelel a minőségbiztosítási kritériumoknak

2026. június 1.

Első közzététel (Tényleges)

2026. június 5.

Tanulmányi rekordok frissítései

Utolsó frissítés közzétéve (Tényleges)

2026. július 29.

Az utolsó frissítés elküldve, amely megfelel a minőségbiztosítási kritériumoknak

2026. július 28.

Utolsó ellenőrzés

2026. július 1.

Több információ

A tanulmányhoz kapcsolódó kifejezések

Terv az egyéni résztvevői adatokhoz (IPD)

Tervezi megosztani az egyéni résztvevői adatokat (IPD)?

IGEN

IPD terv leírása

Upon completion, all study information will be de-identified, and shared with our colleagues at the Centro Cardiologico Monzino (Milan, Italy), Dr. Daniela Trabattoni. Dr. Trabattonia and her colleagues are performing a parallel trial with the same protocol, but using a PFO closure device not available in the United States.

IPD megosztási időkeret

Starting April 2026, all supportive information is being shared collaboratively. No IPD will be shared until the study is completed at both sites (estimated 2028).

IPD-megosztási hozzáférési feltételek

The two principal investigators (Sommer and Trabattoni) will have access to the de-identified data and supporting information, as well as their dedicated research teams. Outcome data from the two sites will be compared and potentially combined into a single report.

Az IPD megosztását támogató információ típusa

  • STUDY_PROTOCOL
  • NEDV
  • ICF
  • ANALYTIC_CODE
  • CSR

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