Меню
Набор скоро начнётся NCT06535022

DeliKet (Substudy of KetoNiFast Study ID 22-1398_1)

Без фазы С лечением Delirium Ketogenic Dieting Nutrition, Healthy

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: Cyclic enteral daytime feeding with ketogenic nighttime fasting and exogenous ketone salt supplementation (ß-hydroxybutyrate).
Кому может быть актуально
Состояния в реестре: Delirium, Ketogenic Dieting, Nutrition, Healthy. 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
Список центров уточняется — проверьте первичный протокол.
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Impact of Cyclic, Daytime Enteral Nutrition and Ketogenic Nighttime Fasting on the Incidence of Postoperative Delirium in Critically Ill Patients

Обзор

Postoperative delirium is a common problem of the critically ill patient and associated with an increased mortality. Intermittent fasting and ketogenesis have been shown to be beneficial for maintaining a circadian rhythm and initiating anti-inflammatory repair mechanisms which could potentially be neuroprotective. However, so far there is little data if cyclic enteral feeding with ketogenic nighttime fasting might be beneficial for reducing the rate of postoperative delirium. The study hypothesis is that equicaloric cyclic enteral feeding (12 hrs) during daytime with ketogenic fasting and exogenous ketone supplementation at nighttime compared to continuous standard enteral nutrition (24 hours) decreases the incidence of postoperative delirium in critically ill patients.

Подробное описание

Postoperative delirium remains a common postoperative problem in critically ill patients with a prevalence of up to 20% and even up to 50% in the elderly population. But postoperative delirium has a negative impact on mortality as several studies were able to show in the past. Therefore, aiming for a reduction of postoperative delirium has an important impact on patients' outcome. One helpful tool for avoiding postoperative delirium is maintaining a circadian pattern. Enteral feeding may play an important role here. Healthy humans have a circadian feeding pattern with nighttime fasting. There is increasing evidence that a circadian rhythm of feeding (cyclic feeding) could be beneficial for critical ill patients. Cyclic feeding and fasting are assumed to have positive effects on the gut microbiome resulting in optimization of host responses to gastrointestinal pathogens. Another positive effect of cyclic feeding potentially results from activation of a "fasting response", inducing repair pathways such as ketogenesis, mitochondrial biogenesis, anti-inflammatory pathways, antioxidant defenses and autophagy processes. The activation of these repair pathways could diminish cellular stress and promote cellular recovery in critical ill patients. This could have a positive effect on postoperative delirium. A randomized controlled trial by van Dyck et al. could show that fasting-mimicking intervals of 12 hours are sufficient to generate a metabolic fasting response without risking a caloric deficit. This fasting response can be enhanced by additional supplementation of exogenous ketones. The study objective is that equicaloric cyclic enteral feeding (for 12 hours) during daytime with ketogenic fasting (for 12 hours) at nighttime (aiming for a ß-hydroxybutyrate blood concentrations ≥ 0.5mM by exogenous ketone supplementation) compared to continuous (for 24 hours) standard enteral nutrition as per patients' nutritional requirements decreases the incidence of postoperative delirium of critically ill patients.

Вмешательства

  • Пищевая добавка Cyclic enteral daytime feeding with ketogenic nighttime fasting and exogenous ketone salt supplementation (ß-hydroxybutyrate)
    Nighttime fasting and ß-hydroxybutyrate supplementation

Первичные конечные точки

  • Confusion Assessment Method (CAM- ICU) [Срок оценки: Day 1-14 after randomization or until ICU discharge]
  • • Montreal Cognitive Assessment (MoCA- Score) [Срок оценки: Day 1-14 after randomization or until ICU- discharge]
  • MMSE (Minimental State Examination) [Срок оценки: Day 1-14 after randomization or until ICU discharge]
Вторичные конечные точки (3)
  • Duration of ventilation [Срок оценки: From day of randomization until ICU discharge up to 1 month]
  • Length of ICU- and Hospital stay [Срок оценки: From day of randomization until hospital discharge up to 6 months]
  • 30-day mortality [Срок оценки: From day of randomization up until 30 days]

Критерии участия

Критерии включения

  • Age ≥ 18 years
  • Admission to an ICU
  • Start of enteral nutrition

Критерии исключения

  • Severe liver insufficiency / liver disease (Child Pugh > B or 7-9 points)
  • Post total Pancreatectomy / Insulin-depending diabetes mellitus (IDDM)
  • Pregnancy / Lactation
  • Hemoglobin-concentration < 80g/l
  • Severe metabolic disorder / severe autoimmune disease
  • Refractory respiratory or metabolic acidosis
  • Disorder of mitochondrial transportation of fatty acids
  • Disorder of the oxidation of fatty acids
  • Disorder of gluconeogenesis, der ketone body production or ketone body degradation
  • Intermittent porphyria
  • Severe arrhythmia / cardiomyopathy
  • Contraindications against enteral nutrition
  • Missing informed consent

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

Список центров уточняется — проверьте первичный протокол.

Идентификаторы

NCT: NCT06535022 · 22-1398_2

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗