Migraine Headaches Elimination With Patent Foramen Ovale-Directed Therapy (COMFORT-PFO)
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?
研究概览
详细说明
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.
研究类型
注册 (估计的)
阶段
- 第三阶段
联系人和位置
学习联系方式
- 姓名:Robert J Sommer, MD
- 电话号码:212-342-0886
- 邮箱:rs2463@cumc.columbia.edu
研究联系人备份
- 姓名:Barbara T Robbins, FNP-BC
- 电话号码:212-342-0886
- 邮箱:bs2575@cumc.columbia.edu
学习地点
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New York
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New York、New York、美国、10032
- Columbia University Irving Medical Center - NewYork Presbyterian Hospital (CUIMC/NYP)
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接触:
- Robert J Sommer, MD
- 电话号码:2123420886
- 邮箱:rs2463@cumc.columbia.edu
-
接触:
- Barbara T Robbins, FNP-BC
- 电话号码:2123420886
- 邮箱:bs2575@cumc.columbia.edu
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首席研究员:
- Robert J Sommer, MD
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参与标准
资格标准
适合学习的年龄
- 成人
接受健康志愿者
描述
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
学习计划
研究是如何设计的?
设计细节
- 主要用途:预防
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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有源比较器: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.
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Six months of daily prasugrel therapy following randomization.
其他名称:
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有源比较器: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.
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Six months of daily prasugrel therapy following randomization.
其他名称:
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.
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Reduction in Monthly Migraine Days (MMD)
大体时间:upon completion of the 56-day Post-Therapy monitoring session
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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).
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upon completion of the 56-day Post-Therapy monitoring session
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Effect Persistence (EP)
大体时间:upon completion of the 56-day Post-Therapy monitoring session
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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
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Responder-based Endpoints
大体时间:upon completion of the 56-day Post-Therapy monitoring session
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Responder-based endpoints will assess higher thresholds of clinical response and will include the proportion of subjects achieving:
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upon completion of the 56-day Post-Therapy monitoring session
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Absolute reduction in MMD from Baseline to Post-Therapy
大体时间:upon completion of the 56-day Post-Therapy monitoring session
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This measure will calculate the absolute difference in MMD between the Baseline monitoring session and the Post-Therapy monitoring session.
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upon completion of the 56-day Post-Therapy monitoring session
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Percent reduction in MMD from Baseline to Post-Therapy
大体时间:upon completion of the 56-day Post-Therapy monitoring session
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This measure will assess the percentage difference in MMD between the Baseline monitoring session and the Post-Therapy session.
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upon completion of the 56-day Post-Therapy monitoring session
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Change in MSQ 2.1 Score (Baseline Score - Post-thienopyridine Score)
大体时间:Baseline and upon completion of the 56-day Post-Therapy monitoring session
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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.
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Baseline and upon completion of the 56-day Post-Therapy monitoring session
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Change in HIT-6 Score (Baseline Score - Post-thienopyridine Score)
大体时间:Baseline and upon completion of the 56-day Post-Therapy monitoring session
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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.
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Baseline and upon completion of the 56-day Post-Therapy monitoring session
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合作者和调查者
调查人员
- 首席研究员:Robert J Sommer, MD、Columbia University
- 首席研究员:Jessica Ailani, MD、MedStar Georgetown University Hospital
出版物和有用的链接
一般刊物
- Saver JL, Carroll JD, Thaler DE, Smalling RW, MacDonald LA, Marks DS, Tirschwell DL; RESPECT Investigators. Long-Term Outcomes of Patent Foramen Ovale Closure or Medical Therapy after Stroke. N Engl J Med. 2017 Sep 14;377(11):1022-1032. doi: 10.1056/NEJMoa1610057.
- Kent DM, Saver JL, Kasner SE, Nelson J, Carroll JD, Chatellier G, Derumeaux G, Furlan AJ, Herrmann HC, Juni P, Kim JS, Koethe B, Lee PH, Lefebvre B, Mattle HP, Meier B, Reisman M, Smalling RW, Soendergaard L, Song JK, Mas JL, Thaler DE. Heterogeneity of Treatment Effects in an Analysis of Pooled Individual Patient Data From Randomized Trials of Device Closure of Patent Foramen Ovale After Stroke. JAMA. 2021 Dec 14;326(22):2277-2286. doi: 10.1001/jama.2021.20956.
- Trabattoni D, Brambilla M, Canzano P, Becchetti A, Teruzzi G, Porro B, Fiorelli S, Muratori M, Tedesco CC, Veglia F, Montorsi P, Bartorelli AL, Tremoli E, Camera M. Migraine in Patients Undergoing PFO Closure: Characterization of a Platelet-Associated Pathophysiological Mechanism: The LEARNER Study. JACC Basic Transl Sci. 2022 Apr 13;7(6):525-540. doi: 10.1016/j.jacbts.2022.02.002. eCollection 2022 Jun.
- Sondergaard L, Kasner SE, Rhodes JF, Andersen G, Iversen HK, Nielsen-Kudsk JE, Settergren M, Sjostrand C, Roine RO, Hildick-Smith D, Spence JD, Thomassen L; Gore REDUCE Clinical Study Investigators. Patent Foramen Ovale Closure or Antiplatelet Therapy for Cryptogenic Stroke. N Engl J Med. 2017 Sep 14;377(11):1033-1042. doi: 10.1056/NEJMoa1707404.
- Wilmshurst PT, Nightingale S, Walsh KP, Morrison WL. Effect on migraine of closure of cardiac right-to-left shunts to prevent recurrence of decompression illness or stroke or for haemodynamic reasons. Lancet. 2000 Nov 11;356(9242):1648-51. doi: 10.1016/s0140-6736(00)03160-3.
- Schwerzmann M, Wiher S, Nedeltchev K, Mattle HP, Wahl A, Seiler C, Meier B, Windecker S. Percutaneous closure of patent foramen ovale reduces the frequency of migraine attacks. Neurology. 2004 Apr 27;62(8):1399-401. doi: 10.1212/01.wnl.0000120677.64217.a9.
- Giardini A, Donti A, Formigari R, Salomone L, Palareti G, Guidetti D, Picchio FM. Long-term efficacy of transcatheter patent foramen ovale closure on migraine headache with aura and recurrent stroke. Catheter Cardiovasc Interv. 2006 Apr;67(4):625-9. doi: 10.1002/ccd.20699.
- Reisman M, Christofferson RD, Jesurum J, Olsen JV, Spencer MP, Krabill KA, Diehl L, Aurora S, Gray WA. Migraine headache relief after transcatheter closure of patent foramen ovale. J Am Coll Cardiol. 2005 Feb 15;45(4):493-5. doi: 10.1016/j.jacc.2004.10.055.
- Slavin L, Tobis JM, Rangarajan K, Dao C, Krivokapich J, Liebeskind DS. Five-year experience with percutaneous closure of patent foramen ovale. Am J Cardiol. 2007 May 1;99(9):1316-20. doi: 10.1016/j.amjcard.2006.12.054. Epub 2007 Mar 20.
- Kimmelstiel C, Gange C, Thaler D. Is patent foramen ovale closure effective in reducing migraine symptoms? A controlled study. Catheter Cardiovasc Interv. 2007 Apr 1;69(5):740-6. doi: 10.1002/ccd.21025.
- Wahl A, Praz F, Tai T, Findling O, Walpoth N, Nedeltchev K, Schwerzmann M, Windecker S, Mattle HP, Meier B. Improvement of migraine headaches after percutaneous closure of patent foramen ovale for secondary prevention of paradoxical embolism. Heart. 2010 Jun;96(12):967-73. doi: 10.1136/hrt.2009.181156.
- Dowson A, Mullen MJ, Peatfield R, Muir K, Khan AA, Wells C, Lipscombe SL, Rees T, De Giovanni JV, Morrison WL, Hildick-Smith D, Elrington G, Hillis WS, Malik IS, Rickards A. Migraine Intervention With STARFlex Technology (MIST) trial: a prospective, multicenter, double-blind, sham-controlled trial to evaluate the effectiveness of patent foramen ovale closure with STARFlex septal repair implant to resolve refractory migraine headache. Circulation. 2008 Mar 18;117(11):1397-404. doi: 10.1161/CIRCULATIONAHA.107.727271. Epub 2008 Mar 3.
- Mattle HP, Evers S, Hildick-Smith D, Becker WJ, Baumgartner H, Chataway J, Gawel M, Gobel H, Heinze A, Horlick E, Malik I, Ray S, Zermansky A, Findling O, Windecker S, Meier B. Percutaneous closure of patent foramen ovale in migraine with aura, a randomized controlled trial. Eur Heart J. 2016 Jul 7;37(26):2029-36. doi: 10.1093/eurheartj/ehw027. Epub 2016 Feb 22.
- Tobis JM, Charles A, Silberstein SD, Sorensen S, Maini B, Horwitz PA, Gurley JC. Percutaneous Closure of Patent Foramen Ovale in Patients With Migraine: The PREMIUM Trial. J Am Coll Cardiol. 2017 Dec 5;70(22):2766-2774. doi: 10.1016/j.jacc.2017.09.1105.
- 11. The ESCAPE Migraine Trial: https://clinicaltrials.gov/study/NCT00267371?cond=Migraine%20Headache&intr=PFO%20Closure&page=2&rank=15
- Kent DM, Thaler DE; RoPE Study Investigators. The Risk of Paradoxical Embolism (RoPE) Study: developing risk models for application to ongoing randomized trials of percutaneous patent foramen ovale closure for cryptogenic stroke. Trials. 2011 Jul 27;12:185. doi: 10.1186/1745-6215-12-185.
- Rodes-Cabau J, Horlick E, Ibrahim R, Cheema AN, Labinaz M, Nadeem N, Osten M, Cote M, Marsal JR, Rivest D, Marrero A, Houde C. Effect of Clopidogrel and Aspirin vs Aspirin Alone on Migraine Headaches After Transcatheter Atrial Septal Defect Closure: The CANOA Randomized Clinical Trial. JAMA. 2015 Nov 24;314(20):2147-54. doi: 10.1001/jama.2015.13919.
- 20. RELIEF Trial: https://clinicaltrials.gov/study/NCT04100135?cond=Migraine%20Headache&term=relief%20clinical%20study&rank=1.
- Safiri S, Pourfathi H, Eagan A, Mansournia MA, Khodayari MT, Sullman MJM, Kaufman J, Collins G, Dai H, Bragazzi NL, Kolahi AA. Global, regional, and national burden of migraine in 204 countries and territories, 1990 to 2019. Pain. 2022 Feb 1;163(2):e293-e309. doi: 10.1097/j.pain.0000000000002275.
- Charleston L 4th, Royce J, Monteith TS, Broner SW, O'Brien HL, Manrriquez SL, Robbins MS. Migraine Care Challenges and Strategies in US Uninsured and Underinsured Adults: A Narrative Review, Part 1. Headache. 2018 Apr;58(4):506-511. doi: 10.1111/head.13286. Epub 2018 Mar 8.
- Spencer BT, Qureshi Y, Sommer RJ. A retrospective review of clopidogrel as primary therapy for migraineurs with right to left shunt lesions. Cephalalgia. 2014 Oct;34(11):933-7. doi: 10.1177/0333102414523845. Epub 2014 Apr 25.
- Reisman AM, Robbins BT, Chou DE, Yugrakh MS, Gross GJ, Privitera L, Nazif T, Sommer RJ. Ticagrelor for Refractory Migraine/Patent Foramen Ovale (TRACTOR): An open-label pilot study. Neurology. 2018 Nov 27;91(22):1010-1017. doi: 10.1212/WNL.0000000000006573.
- Sommer RJ, Robbins BT. Migraine Headache and Patent Foramen Ovale: Observational Studies, the Randomized Clinical Trials, and the GORE RELIEF Clinical Study. Cardiol Clin. 2024 Nov;42(4):497-507. doi: 10.1016/j.ccl.2024.01.007. Epub 2024 Feb 29.
- Sommer RJ, Nazif T, Privitera L, Robbins BT. Retrospective review of thienopyridine therapy in migraineurs with patent foramen ovale. Neurology. 2018 Nov 27;91(22):1002-1009. doi: 10.1212/WNL.0000000000006572.
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- ACYY2573
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
IPD 共享时间框架
IPD 共享访问标准
IPD 共享支持信息类型
- 研究方案
- 树液
- 国际碳纤维联合会
- 分析代码
- 企业社会责任
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