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

2026年7月28日 更新者: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?

調査の概要

状態

まだ募集していません

条件

介入・治療

詳細な説明

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.

研究の種類

介入

入学 (推定)

32

段階

  • フェーズ 3

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

研究場所

    • New York
      • New York、New York、アメリカ、10032
        • Columbia University Irving Medical Center - NewYork Presbyterian Hospital (CUIMC/NYP)
        • コンタクト:
        • コンタクト:
        • 主任研究者:
          • Robert J Sommer, MD

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人

健康ボランティアの受け入れ

いいえ

説明

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

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:防止
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
アクティブコンパレータ: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.
他の名前:
  • Prasugrel Hydrochloride
アクティブコンパレータ: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.
他の名前:
  • 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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Reduction in Monthly Migraine Days (MMD)
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
Effect Persistence (EP)
時間枠: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
時間枠: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
時間枠: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
時間枠: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)
時間枠: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)
時間枠: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

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

協力者

捜査官

  • 主任研究者:Robert J Sommer, MD、Columbia University
  • 主任研究者:Jessica Ailani, MD、MedStar Georgetown University Hospital

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

一般刊行物

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年9月1日

一次修了 (推定)

2027年12月1日

研究の完了 (推定)

2028年3月1日

試験登録日

最初に提出

2026年5月22日

QC基準を満たした最初の提出物

2026年6月1日

最初の投稿 (実際)

2026年6月5日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月29日

QC基準を満たした最後の更新が送信されました

2026年7月28日

最終確認日

2026年7月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • ACYY2573

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

はい

IPD プランの説明

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 共有時間枠

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 共有アクセス基準

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.

IPD 共有サポート情報タイプ

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • ANALYTIC_CODE
  • CSR

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