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Идёт набор NCT03636295

Low INR to Minimize Bleeding With Mechanical Valves Trial

Фаза III С лечением Bleeding Post-mechanical Valve Replacement Thromboembolism Post-mechanical Valve Replacement

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: Warfarin.
Кому может быть актуально
Состояния в реестре: Bleeding Post-mechanical Valve Replacement, Thromboembolism Post-mechanical Valve Replacement. 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
Бельгия, Botswana, Бразилия, Cameroon, Канада +12
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

Обзор

This study evaluates the use of a lower INR target (1.5 to 2.5) in patients with a mechanical bileaflet heart valve in the aortic position. This study will inform physicians about whether a lower INR target will decrease the risk of bleeding or increase the risk of blood clot formation and stroke. These results have the potential to reduce the burden of bleeding in patients with a mechanical heart valve who require lifelong warfarin (Coumadin) treatment.

Подробное описание

Warfarin (Coumadin) is a blood thinner used to prevent blood clot formation in patients with mechanical heart valves. Blood clots can block blood flow to the brain, heart, or other parts of the body. Mechanical heart valves increases the risk of clot so patients with a mechanical heart valve must take warfarin to reduce their risk of stroke and other blood clot-related problems.

The degree to which warfarin 'works' varies from person to person, and so dosage is determined by measuring each person's response to the drug as an 'international normalized ratio' or INR. A patient with an INR over 1.0 has blood that takes longer to clot than average, and increasing INR values represent increasing time required for blood to clot. While an INR over 1.0 decreases clotting risk, it also increases bleeding risk. It is important to carefully balance these risks.

Specific INR targets have been recommended for patients with a mechanical heart valve, but these recommendations differ between scientific groups and are based on low quality evidence. Recent studies suggest that a lower INR target range than is currently recommended can be used safely. A laboratory study showed that warfarin effectively prevents blood clot formation on mechanical heart valves as long as the INR is 1.5 or above. Two moderately-sized clinical studies showed that an INR target range of 1.5-2.5 resulted in less bleeding than the usual higher target range without increasing blood clot formation or stroke in patients with a newer valve model. Whether we could use a lower INR target range for patients with a mechanical aortic valve remains controversial.

This study evaluates the use of a lower INR target (1.5 to 2.5) in patients with a mechanical bileaflet heart valve in the aortic position. This study will inform physicians about whether a lower INR target will decrease the risk of bleeding or increase the risk of blood clot formation and stroke. These results have the potential to reduce the burden of bleeding in patients with a mechanical heart valve who require lifelong warfarin (Coumadin) treatment.

Вмешательства

  • Препарат Warfarin
    Participants in both arms will be on warfarin therapy post-mechanical valve replacement as is standard, but will have different INR target ranges.

Первичные конечные точки

  • Thrombosis/thromboembolism [Срок оценки: Through study completion, an expected mean of 2-3 years]
  • Major bleeding [Срок оценки: Through study completion, an expected mean of 2-3 years]
Вторичные конечные точки (12)
  • All cause mortality [Срок оценки: Through study completion, an expected mean of 2-3 years]
  • All clinically important bleeding [Срок оценки: Through study completion, an expected mean of 2-3 years]
  • Minor bleeding [Срок оценки: Through study completion, an expected mean of 2-3 years]
  • All stroke [Срок оценки: Through study completion, an expected mean of 2-3 years]
  • Ischemic stroke [Срок оценки: Through study completion, an expected mean of 2-3 years]
  • Hemorrhagic stroke [Срок оценки: Through study completion, an expected mean of 2-3 years]
  • Type 1, 2 or 3 myocardial infarction [Срок оценки: Through study completion, an expected mean of 2-3 years]
  • Systemic thromboembolism [Срок оценки: Through study completion, an expected mean of 2-3 years]
  • Valve thrombosis [Срок оценки: Through study completion, an expected mean of 2-3 years]
  • Pulmonary embolism [Срок оценки: Through study completion, an expected mean of 2-3 years]
  • Deep vein thrombosis [Срок оценки: Through study completion, an expected mean of 2-3 years]
  • New renal replacement therapy [Срок оценки: Through study completion, an expected mean of 2-3 years]

Критерии участия

Критерии включения

  • Age is 18 or older at the time of enrolment
  • Have had a bileaflet mechanical heart valve implant in the aortic position 3 or more months ago
  • Written informed consent from either the patient or substitute decision maker

Критерии исключения

  • Has a second implanted mechanical valve (any position)
  • Lower boundary of planned INR range is less than 2.0
  • Pregnant or expecting to become pregnant during the study follow-up

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Лечение

Центры проведения

Бразилия · 5 центров
  • Sociedade Hospitalar Angelina Caron — Campina Grande do Sul
  • HEW Cardiologia LTDA — Joinville
  • InCor-HCFMUSP — Cerqueira César
  • Fundação Universitária de Cardiologia mantededora do Instituto de Cardiologia e Transplant — Brasília
  • Dante Pazzanese Institute of Cardiology — São Paulo
Канада · 5 центров
  • Nova Scotia Health Authority — Halifax
  • Hamilton General Hospital — Hamilton
  • London Health Sciences Centre Research Inc. — London
  • The Ottawa Hospital Research Institute — Ottawa
  • Jewish General Hospital — Montreal
Бельгия · 4 центра
  • Ziekenhuis Oost-Limburg — Genk
  • AZ Oostende — Ostend
  • Imelda Hospital — Keerbergen
  • Universitair Ziekenhuis Leuven — Leuven
Дания · 3 центра
  • Esbjerg & Grindsted Hospital - University Hospital of Southern Denmark — Esbjerg
  • Southern Jutland Hospital — Aabenraa
  • Aarhus University Hospital — Aarhus
Nepal · 3 центра
  • Shahid Gangalal National Heart Centre — Kathmandu
  • Nobel Medical College and Teaching Hospital — Biratnagar
  • BP Koirala Institute of Health Sciences — Dharān
Великобритания · 3 центра
  • Golden Jubilee National Hospital — Clydebank
  • Liverpool Heart & Chest Hospital — Liverpool
  • South Tees Hospitals NHS Foundation Trust of The James Cook University Hospital — Middlesbrough
Италия · 2 центра
  • Città di Lecce Hospital — Lecce
  • Azienda Ospedaliero Universitaria Policlinico Riuniti Foggia — Foggia
Botswana · 1 центр
  • University of Botswana, at Princess Marina Hospital — Gaborone
Cameroon · 1 центр
  • St. Elizabeth Catholic General Hospital — Kumbo
Китай · 1 центр
  • Fuwai Hospital, CAMS & PUMC — Пекин
Германия · 1 центр
  • Universitätsklinikum Jena — Jena
Нидерланды · 1 центр
  • Erasmus University Medical Centre — Rotterdam
Пакистан · 1 центр
  • Shifa Clinical Research Center — Islamabad
Россия · 1 центр
  • Meshalkin National Medical Research Center — Novosibirsk
Саудовская Аравия · 1 центр
  • King Faisal Specialist Hospital & Research Centre — Riyadh
South Korea · 1 центр
  • Soonchunhyang University Gumi Hospital — Gumi
Испания · 1 центр
  • Hospital de la Santa Creu i Sant Pau — Barcelona

Публикации

  • Puskas J, Gerdisch M, Nichols D, Quinn R, Anderson C, Rhenman B, Fermin L, McGrath M, Kong B, Hughes C, Sethi G, Wait M, Martin T, Graeve A; PROACT Investigators. Reduced anticoagulation after mechanical aortic valve replacement: interim results from the prospective randomized on-X valve anticoagulation clinical trial randomized Food and Drug Administration investigational device exemption trial. PMID 24512654
  • Torella M, Torella D, Chiodini P, Franciulli M, Romano G, De Santo L, De Feo M, Amarelli C, Sasso FC, Salvatore T, Ellison GM, Indolfi C, Cotrufo M, Nappi G. LOWERing the INtensity of oral anticoaGulant Therapy in patients with bileaflet mechanical aortic valve replacement: results from the "LOWERING-IT" Trial. Am Heart J. 2010 Jul;160(1):171-8. doi: 10.1016/j.ahj.2010.05.005. PMID 20598989

Идентификаторы

NCT: NCT03636295 · 5139

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗