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Набор скоро начнётся NCT07064135

Improved Medication and Care to Achieve Lipid Targets After Carotid Surgery

Без фазы С лечением Dyslipidaemias Carotid Artery Stenoses

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: Prompt Medication Adjustment and Intensive Follow-up, Standard Care.
Кому может быть актуально
Состояния в реестре: Dyslipidaemias, Carotid Artery Stenoses. 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
Австрия
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Impact of Prompt Medication Adjustment and Intensive Follow-up on Achieving Lipid Targets in Patients Undergoing Carotid Endarterectomy

Обзор

The goal of this clinical trial is to find out if patients who receive extra support stay on their cholesterol-lowering therapy and therefore have lower cholesterol levels after 4 months. Extra support means regular phone calls and close monitoring before and after carotid artery surgery. The study compares this approach to usual care. Participants will: Be randomly assigned to either standard care or extra support for 4 months. Receive cholesterol-lowering treatment and attend follow-up visits.

Подробное описание

Cardiovascular risk factors are one of the leading causes of morbidity and mortality worldwide. Improving these often fails due to the lack of low-threshold access to specialized medical care. Especially in vascular surgery departments with multimorbid patients, optimizing the management of risk factors-particularly cholesterol-is essential.

This exploratory randomized controlled pilot study aims to investigate the effects of pharmacological optimization of cholesterol management after carotid surgery with subsequent follow-up visits. For this purpose, 50 patients who are undergoing carotid surgery due to carotid stenosis will be randomized into two groups. In Group 1, 25 patients who have not reached the lipid target at the time of surgery will be included and re-evaluated regarding their therapy after 2 months and undergo another ambulatory cholesterol check after 4 months. In Group 2, 25 patients who also have not reached the lipid target at the time of surgery will be included and, after optimization of therapy during the hospital stay, will undergo an ambulatory cholesterol check after 4 months.

Вмешательства

  • Поведенческое Prompt Medication Adjustment and Intensive Follow-up
    Participants receive prompt adjustment of lipid-lowering therapy perioperatively and 6-8 weeks after carotid endarterectomy to achieve guideline-recommended LDL-C targets, combined with intensive follow-up visits and laboratory monitoring. Intensive follow-up visits and laboratory monitoring of lipid parameters are performed at 6-8 weeks and again at 12-16 weeks postoperatively to optimize lipid management.
  • Другое Standard Care
    Participants receive standard postoperative care according to guidelines, including lipid management and routine follow-up without additional early intervention or intensive monitoring. Lipid parameters are assessed only once at 12-16 weeks postoperatively.

Первичные конечные точки

  • Proportion of patients achieving the LDL-C target of <55 mg/dL [Срок оценки: 12-16 weeks]

Критерии участия

Критерии включения

  • Age >17 years
  • Diagnosed carotid artery stenosis
  • Planned carotid endarterectomy
  • LDL cholesterol >55 mg/dL
  • Willingness to participate, documented by written informed consent

Критерии исключения

  • Ongoing treatment with PCSK9 inhibitors
  • Carotid surgery for reasons other than stenosis (e.g., traumatic injury)

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
Поддерживающая терапия

Центры проведения

Австрия · 1 центр
  • Konventhospital Barmherzige Brüder — Linz

Идентификаторы

NCT: NCT07064135 · IMACS-2025

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗