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Набор по приглашению NCT06108102

International Post-Stroke Epilepsy Research Repository

Наблюдательное Post Stroke Epilepsy Post Stroke Seizure Stroke Epilepsy

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Presence of stroke, either ischemic or hemorrhagic (intracerebral and subarachnoid).
Кому может быть актуально
Состояния в реестре: Post Stroke Epilepsy, Post Stroke Seizure, Stroke, Epilepsy. Базовые параметры: от 18 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
США
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

International Post Stroke Epilepsy Research Repository to Characterize Post-stroke Epilepsy Population and Their Outcomes

Обзор

The International Post-Stroke Epilepsy Research Repository (IPSERR): The study aims to collate and categorize data reported by post-stroke epilepsy (PSE) researchers and lodge it within the IPSERR. Using the IPSERR database, we will conduct two individual patient data (IPD) analyses: (1) determine epilepsy, functional, and cognitive outcomes in stroke patients who develop post-stroke seizure and (2) build and validate post-stroke epilepsy prediction model and compare performance against existing models.

Подробное описание

The cerebrovascular disease is the most common cause of late-onset epilepsy. PSE is associated with increased morbidity, including cognitive decline, dependence, and poor quality of life, and is a critical determinant factor of stroke prognosis. We recently reported a systematic review and meta-analysis of 71 papers that suggested that post-stroke seizures are associated with more significant mortality and poor functional and cognitive outcomes (PMID:37721736). In this study, we observed disparate methods used by the individual investigators. We also noted variations in study reporting. PI aims to analyze existing individual patient data, including those analyzed in the systematic review, by collaborating with colleagues in the field and developing IPSERR into a resource for future collaborative studies that will tackle anti-epileptogenesis drug trial design.

Design and Rationale:

1. International Post-Stroke Epilepsy Research Repository (IPSERR): The PI convened the International Post-Stroke Epilepsy Research Consortium (IPSERC) with co-convenor Dr. Patrick Kwan, Monash University, Australia. IPSERR was subsequently founded to collect retrospective and prospective PSE data to promote all aspects of PSE research. Participating centers will obtain legal approvals for human subject research as per the requirements of their jurisdiction. The PI (NKM) has IRB approval for IPSERR. A data use agreement (DUA) will be executed to receive data. The PI will invite the authors of all 71 papers in the systematic review to join IPSERC and request them to contribute data to IPSERR. A protocol (including the charter) for the proposed IPD analyses has been accepted for publication and will be available to the collaborators for review. 2. The PI will use the Yale Center for Research Computing (YCRC) resources to manage IPSERR's clinical, radiological, and electrophysiological data. 3. The PI will use Redcap for clinical data management. The Redcap server is housed within the Yale-New Haven Hospital secured data center behind their firewall. The databases are encrypted at rest for HIPAA compliance. Full database backups are made twice daily, seven days a week. 4. Study duration: 2023-2029 5. Rationale: Collaboration is vital for PSE research. This is because approximately 10% of stroke patients develop PSE. Together, investigators can collect a large sample of the PSE patient population and conduct robust analyses to draw meaningful conclusions. The collation of IPD from many different sources involving different interventions and stroke subpopulations will strengthen our ability to provide data for future research on many topics relating to PSE. The availability of high-speed internet has made it easier than ever to work closely with colleagues worldwide and share data. There are many examples of such successful efforts. For example, PI Dr. Mishra closely worked with the SITS-ISTR registry at Karolinska University, Stockholm, and the Virtual Stroke Trials Archive (VISTA) at the University of Glasgow, UK. These two international efforts recorded tPA and stroke trial data, respectively, and provided them for testing several hypotheses. Dr. Mishra subsequently worked at the US FDA, where he was exposed to other large collaborative scientific efforts like MDEpiNET. The PI seeks to capitalize on his experiences, network of colleagues worldwide, and recent technological advancement in data science to build the IPSERR. We anticipate that the IPSERR will bring together large datasets from previously conducted PSE research that would otherwise ordinarily remain dormant. The PI will request data from the authors of papers included in the systematic review (N=71 papers reporting approximately 20000 PSE patient data) and from the IPSERC members. The PI will report IPSERR in the first year and the results of the two research projects anchored on it in the second year. The PI will recognize that not all authors of the previously published literature in our systematic review will have data to share. However, even if 20% of the patient data is obtained from those studies, the PI expects an extensive database of approximately 8000 patients. With this success, the PI expects the IPSERR to continue growing. IPSERR will catalytically advance PSE research because it will provide the PSE research community with an extensive database for hypotheses testing and a framework to anchor future prospective studies.

Вмешательства

  • Другое Presence of stroke, either ischemic or hemorrhagic (intracerebral and subarachnoid)
    Presence of ischemic or hemorrhagic stroke confirmed by neuroimaging and clinical diagnosis

Первичные конечные точки

  • Mortality (modified Rankin Scale = 6) [Срок оценки: At 1 year, 2 year, and 5 year follow-up]
  • Poor functional outcome (modified Rankin Scale 3-6) [Срок оценки: At 1 year, 2 year, and 5 year follow-up]
  • Seizure frequency [Срок оценки: At 1 year, 2 year, and 5 year follow-up]
  • Seizure severity [Срок оценки: At 1 year, 2 year, and 5 year follow-up]
  • Occurrence or frequency of status epilepticus [Срок оценки: At 1 year, 2 year, and 5 year follow-up]
  • Length of hospital stay [Срок оценки: At 1 year, 2 year, and 5 year follow-up]
  • Cognitive decline assessed on an 11-question Mini-Mental State Examination (MMSE) tool or a 30-point Montreal Cognitive Assessment (MoCA) scale [Срок оценки: At 1 year, 2 year, and 5 year follow-up]
Вторичные конечные точки (5)
  • Recurrent stroke [Срок оценки: At 1 year, 2 year, and 5 year follow-up]
  • Antiseizure medication discontinuation [Срок оценки: At 1 year, 2 year, and 5 year follow-up]
  • Treatment adverse events [Срок оценки: At 1 year, 2 year, and 5 year follow-up]
  • Depression assessed on 21-item Hamilton Depression Rating Scale (HAM-D) [Срок оценки: At 1 year, 2 year, and 5 year follow-up]
  • Anxiety assessed on 14-item Hamilton Anxiety Rating Scale (HAM-A) [Срок оценки: At 1 year, 2 year, and 5 year follow-up]

Критерии участия

Критерии включения

  • Studies with minimum dataset of 100 patients
  • Studies comprising stroke patients aged ≥18 years, with ischemic or hemorrhagic stroke, presenting early or late PSS with data on patient outcome measures.
  • Documented consent or waiver of consent following local Institutional Review Board-approved procedure.
  • Studies published on human subjects.
  • No restriction based on the date or language of publication, gender, or ethnicity.

Критерии исключения

  • Studies of patients with a prior history of seizures before the index stroke,
  • Studies that did not report outcome data, or are not able to share IPD.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения
Случай-контроль

Центры проведения

США · 1 центр
  • Yale University — New Haven

Публикации

  • Mishra NK, Kwan P, Tanaka T, Sunnerhagen KS, Dawson J, Zhao Y, Misra S, Wang S, Sharma VK, Mazumder R, Funaro MC, Ihara M, Nicolo JP, Liebeskind DS, Yasuda CL, Cendes F, Quinn TJ, Ge Z, Scalzo F, Zelano J, Kasner SE; International Post-Stroke Epilepsy Research Consortium (IPSERC); International Post Stroke Epilepsy Research Consortium (IPSERC). Clinical characteristics and outcomes of patients wit PMID 37968000

Идентификаторы

NCT: NCT06108102 · 2000032731 · No NIH funding

Первоисточники (государственные реестры)

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