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Идёт набор NCT07378137

Comparing the Components of Composite Endpoints for Healthcare Providers and Patients

Наблюдательное Coronary Artery Disease Percutaneous Coronary Intervention

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: Questionnaire.
Кому может быть актуально
Состояния в реестре: Coronary Artery Disease, Percutaneous Coronary Intervention. 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
Китай
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

A Preference Study Comparing the Components of Composite Endpoints for Healthcare Providers and Patients With CAD

Обзор

Clinical trials often employ a composite primary endpoint to increase event rates and enhance trial efficiency. However, analytic approaches to composite endpoints typically assume that the individual components are of similar importance. In practice, a treatment often has different effects on each individual endpoint, leading to uncertainty in interpreting the results of a clinical trial employing a composite primary endpoint. Some investigators have recommended using a weighted composite endpoint to address these concerns, in which individual components are valued relative to one another. However, data to inform the weighting of individual endpoints, using opinions from both medical staff and patients, remains controversial. Furthermore, prior efforts to weigh composite endpoints have assumed that patients, physicians, and clinical trialists would assign similar values to individual events. If patients value endpoints differently from trialists, this would suggest that efforts to develop weighted composite endpoints may also need to address patient preferences. In the current study, we aim to record the weighing of both patients and medical staff towards a composite endpoint frequently used in cardiovascular clinical trials. To better understand the value of each endpoint for patients and medical staff, we quantified the relative severity of each endpoint when compared to death and assessed for rating differences between the two groups. Additionally, we investigated whether endpoint weights varied by the demographic and clinical characteristics of patients and medical staff.

Вмешательства

  • Другое Questionnaire
    A questionnaire regarding the weights given by the patients with CAD and the medical staff for the individual components of the composite endpoint

Первичные конечные точки

  • Relative weight of myocardial infarction to death [Срок оценки: Before discharge]
  • Relative weight of stroke to death [Срок оценки: Before discharge]
  • Relative weight of cardiopulmonary resuscitation to death [Срок оценки: Before discharge]
  • Relative weight of procedural complications to death [Срок оценки: Before discharge]
  • Relative weight of major bleeding events to death [Срок оценки: Before discharge]
  • Relative weight of acute kidney injury to death [Срок оценки: Before discharge]
  • Relative weight of revascularization to death [Срок оценки: Before discharge]
  • Relative weight of rehospitalization to death [Срок оценки: Before discharge]

Критерии участия

Критерии включения

  • Patients with acute or chronic coronary syndrome who have undergone percutaneous coronary intervention;
  • Patients who can understand the purpose of this trial and are willing to participate in the preference questionnaire.
  • Healthcare providers who treat patients with coronary artery disease.

Критерии исключения

  • Aged < 18 years;
  • Inability to understand the questionnaire or presence of cognitive impairment.

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

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения
Когортное

Центры проведения

Китай · 1 центр
  • Xijing Hospital — Сиань

Идентификаторы

NCT: NCT07378137 · REC-CHARTENDS

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗