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Идёт набор NCT05845489

Harmonizing Optimal Strategy for Treatment of Coronary Artery Stenosis- CloPidogREl for Primary preVENTION (HOST-PREVENTION)

Фаза IV С лечением Coronary Artery Disease

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: Clopidogrel treatment group, No antiplatelet or anticoagulant group.
Кому может быть актуально
Состояния в реестре: Coronary Artery Disease. Базовые параметры: от 40 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
South Korea
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Efficacy and Safety of Clopidogrel for Primary Prevention in Patients With Subclinical Coronary Atherosclerosis Identified on Imaging

Обзор

The investigators will evaluate the efficacy and safety of clopidogrel for primary prevention in patients diagnosed with coronary atherosclerosis on imaging that did not require revascularization therapy. The trial will test the hypothesis that clopidogrel is beneficial in preventing major adverse cardiovascular and cerebrovascular events (MACCE) in patients with subclinical coronary atherosclerosis identified on imaging.

Подробное описание

Coronary artery disease (CAD) is the most prevalent and lethal disease worldwide. Even though various studies have been performed regarding the prevention or treatment of CAD and its related cardiovascular events, the prevalence of CAD and the incidence of cardiovascular events are increasing.

Antiplatelet agents are among the most widely used drugs for preventing cardiovascular events. The efficacy of antiplatelet agents has been extensively proven in secondary prevention for cardiovascular events in CAD patients, and their use has been recommended in current guidelines. However, there is still controversy surrounding the prescription of antiplatelet agents for the primary prevention of cardiovascular events in CAD patients due to their unknown clear efficacy and risk of bleeding complications.

Recent studies reported the limited efficacy of aspirin in old patients, diabetes patients, or patients with cardiovascular events risks. However, the efficacy or safety of antiplatelet therapy in patients with subclinical coronary atherosclerosis has not been thoroughly investigated. These patients are at higher risk of cardiac death or myocardial infarction compared to patients without coronary atherosclerosis.

In this regard, the investigators will evaluate the efficacy and safety of clopidogrel for primary prevention in patients diagnosed with coronary atherosclerosis on imaging that did not require revascularization therapy.

Вмешательства

  • Препарат Clopidogrel treatment group
    Patients assigned to the clopidogrel treatment group will maintain clopidogrel 75mg once a day for at least 5 years.
  • Другое No antiplatelet or anticoagulant group
    Patients assigned to the no antiplatelet or anticoagulant group will not prescribe antithrombotics for at least 5 years. However, when there is a medical need for antithrombotic therapy during the follow-up, the prescription of antithrombotics is permitted with reporting to the research board.

Первичные конечные точки

  • Major adverse cardiovascular and cerebrovascular events (MACCE) [Срок оценки: at 2 years after the last enrollment]
Вторичные конечные точки (11)
  • Major adverse cardiovascular and cerebrovascular events (MACCE) [Срок оценки: at 5 years after the last enrollment]
  • Net adverse clinical event [Срок оценки: at 2 years and 5 years after the last enrollment]
  • All-cause death [Срок оценки: at 2 years and 5 years after the last enrollment]
  • Non-fatal myocardial infarction [Срок оценки: at 2 years and 5 years after the last enrollment]
  • Any coronary revascularization [Срок оценки: at 2 years and 5 years after the last enrollment]
  • Ischemic stroke or Transient ischemic attack [Срок оценки: at 2 years and 5 years after the last enrollment]
  • Any non-coronary revascularization [Срок оценки: at 2 years and 5 years after the last enrollment]
  • Major bleeding events [Срок оценки: at 2 years and 5 years after the last enrollment]
  • BARC type 2 bleeding events [Срок оценки: at 2 years and 5 years after the last enrollment]
  • BARC type 3 bleeding events [Срок оценки: at 2 years and 5 years after the last enrollment]
  • BARC type 5 bleeding events [Срок оценки: at 2 years and 5 years after the last enrollment]

Критерии участия

Критерии включения

  • Male or female aged ≥40 years
  • Patients with subclinical coronary atherosclerosis identified from coronary CT angiography or coronary angiography within 2 years without clinical events after an imaging study
  • Without significant coronary artery stenosis (Diameter stenosis >50%), which needs revascularization
  • Agreement to give written informed consent

Критерии исключения

  • A history of a diagnosed cardiovascular or cerebrovascular disease (Type1 myocardial infarction, heart failure, peripheral artery disease, stroke, transient ischemic attack, carotid artery stenosis>50%, carotid artery intervention)
  • A history of coronary artery intervention or coronary artery bypass graft surgery, which needs chronic maintenance of antiplatelet therapy
  • Absolute contraindication or allergy to clopidogrel
  • Patients receiving anticoagulants for other comorbidities
  • A history of Bleeding diathesis, known coagulopathy, or major bleeding, BARC class ≥3, resulting in the stop of antiplatelet agents
  • Planned surgery or intervention which needs to stop antiplatelet agents ≥1 month
  • Presence of non-cardiac comorbidity with life expectancy ≤ 5 years at randomization
  • Females with pregnancy or breast-feeding
  • Patients who are thought to be inappropriate for the trial based on physicians' decision

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
Профилактика

Центры проведения

South Korea · 61 центр
  • Seoul National University Hospital — Seoul
  • Andong Hospital — Andong
  • Dong-A University Hospital — Busan
  • Inje University Busan Paik Hospital — Busan
  • Kosin University Gospel Hospital — Busan
  • Pusan National University Hospital — Busan
  • Gyeongsang National University Changwon Hospital — Changwon
  • Soonchunhyang University Cheonan Hospital — Cheonan
  • … и ещё 53 центра

Публикации

  • Yazdanyar A, Newman AB. The burden of cardiovascular disease in the elderly: morbidity, mortality, and costs. Clin Geriatr Med. 2009 Nov;25(4):563-77, vii. doi: 10.1016/j.cger.2009.07.007. PMID 19944261
  • Hennekens CH, Dyken ML, Fuster V. Aspirin as a therapeutic agent in cardiovascular disease: a statement for healthcare professionals from the American Heart Association. Circulation. 1997 Oct 21;96(8):2751-3. doi: 10.1161/01.cir.96.8.2751. No abstract available. PMID 9355934
  • Ajani UA, Ford ES, Greenland KJ, Giles WH, Mokdad AH. Aspirin use among U.S. adults: Behavioral Risk Factor Surveillance System. Am J Prev Med. 2006 Jan;30(1):74-7. doi: 10.1016/j.amepre.2005.08.042. PMID 16414427
  • Ittaman SV, VanWormer JJ, Rezkalla SH. The role of aspirin in the prevention of cardiovascular disease. Clin Med Res. 2014 Dec;12(3-4):147-54. doi: 10.3121/cmr.2013.1197. Epub 2014 Feb 26. PMID 24573704
  • Neumann FJ, Sousa-Uva M, Ahlsson A, Alfonso F, Banning AP, Benedetto U, Byrne RA, Collet JP, Falk V, Head SJ, Juni P, Kastrati A, Koller A, Kristensen SD, Niebauer J, Richter DJ, Seferovic PM, Sibbing D, Stefanini GG, Windecker S, Yadav R, Zembala MO; ESC Scientific Document Group. 2018 ESC/EACTS Guidelines on myocardial revascularization. Eur Heart J. 2019 Jan 7;40(2):87-165. doi: 10.1093/eurhear PMID 30165437
  • McNeil JJ, Wolfe R, Woods RL, Tonkin AM, Donnan GA, Nelson MR, Reid CM, Lockery JE, Kirpach B, Storey E, Shah RC, Williamson JD, Margolis KL, Ernst ME, Abhayaratna WP, Stocks N, Fitzgerald SM, Orchard SG, Trevaks RE, Beilin LJ, Johnston CI, Ryan J, Radziszewska B, Jelinek M, Malik M, Eaton CB, Brauer D, Cloud G, Wood EM, Mahady SE, Satterfield S, Grimm R, Murray AM; ASPREE Investigator Group. Effe PMID 30221597
  • ASCEND Study Collaborative Group; Bowman L, Mafham M, Wallendszus K, Stevens W, Buck G, Barton J, Murphy K, Aung T, Haynes R, Cox J, Murawska A, Young A, Lay M, Chen F, Sammons E, Waters E, Adler A, Bodansky J, Farmer A, McPherson R, Neil A, Simpson D, Peto R, Baigent C, Collins R, Parish S, Armitage J. Effects of Aspirin for Primary Prevention in Persons with Diabetes Mellitus. N Engl J Med. 2018 PMID 30146931
  • Gaziano JM, Brotons C, Coppolecchia R, Cricelli C, Darius H, Gorelick PB, Howard G, Pearson TA, Rothwell PM, Ruilope LM, Tendera M, Tognoni G; ARRIVE Executive Committee. Use of aspirin to reduce risk of initial vascular events in patients at moderate risk of cardiovascular disease (ARRIVE): a randomised, double-blind, placebo-controlled trial. Lancet. 2018 Sep 22;392(10152):1036-1046. doi: 10.101 PMID 30158069

Идентификаторы

NCT: NCT05845489 · H-2212-044-1385

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗