Меню
Идёт набор NCT07616245

MCT Enteral Feeding to Reduce Chyle Leak After Oesophagectomy

Без фазы С лечением Oesphageal Cancer

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: Standard Jejunostomy Feed (Nutrison Protein Plus), MCT-Based Jejunostomy Feed (Nutrison Peptisorb).
Кому может быть актуально
Состояния в реестре: Oesphageal Cancer. 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
Ирландия
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

Обзор

Chyle leak (chylothorax) is a recognised complication following minimally invasive oesophagectomy for oesophageal cancer and may result in prolonged hospital stay, nutritional compromise, and need for additional interventions. Medium-chain triglyceride (MCT) feeds reduce lymphatic flow as they are absorbed directly via the portal circulation rather than through the thoracic duct. While MCT feeds are commonly used in the management of established chyle leaks, their role in prevention has not been evaluated in a randomised controlled trial. This single-centre randomised controlled trial will evaluate whether initiating postoperative jejunostomy feeding with MCT-based enteral nutrition reduces the incidence of clinically and biochemically confirmed chyle leak compared with standard enteral feeding in patients undergoing minimally invasive or robotic-assisted oesophagectomy. Participants will be randomised in a 1:1 ratio to receive either MCT-based feeds or standard jejunostomy feeds starting on postoperative day 1. The primary outcome is the incidence of chylothorax. Secondary outcomes include chest drain output, re-intervention rates, and length of hospital stay.

Подробное описание

Oesophagectomy is a key component of curative treatment for oesophageal cancer. Minimally invasive and robotic-assisted techniques are increasingly used and are associated with improved postoperative recovery. However, these approaches may be associated with a higher incidence of postoperative chyle leak due to extensive mediastinal lymphatic dissection.

Chylothorax occurs when the thoracic duct or its tributaries are disrupted, resulting in leakage of lymphatic fluid into the pleural cavity. This complication can lead to prolonged hospitalisation, nutritional depletion, immunosuppression, and may require radiological or surgical intervention.

Standard postoperative care includes initiation of jejunostomy feeding on postoperative day 1 using enteral formulations containing long-chain triglycerides. These lipids are absorbed via chylomicron formation and transported through the lymphatic system, potentially increasing thoracic duct flow and chyle production.

Medium-chain triglycerides (MCTs), in contrast, are absorbed directly into the portal venous system and bypass the lymphatic circulation. MCT-based feeds are widely used in the management of established chyle leaks, but their prophylactic use has not been evaluated in prospective randomised studies.

This study is a prospective, single-centre, randomised controlled trial conducted at Beaumont Hospital. Adult patients undergoing minimally invasive or robotic-assisted oesophagectomy with placement of a feeding jejunostomy will be eligible for inclusion.

Participants will be randomised in a 1:1 ratio to receive either:

* Standard jejunostomy feeding (Nutrison Protein Plus 1.25 kcal/ml), or * MCT-based jejunostomy feeding (Nutrison Peptisorb 1 kcal/ml)

Enteral feeding will commence on postoperative day 1 and follow an identical escalation protocol in both groups.

The primary endpoint is the incidence of clinically and biochemically confirmed chylothorax, defined according to Esophageal Complications Consensus Group criteria.

Secondary endpoints include:

* Chest drain output volume * Requirement for re-intervention (radiological or surgical) * Postoperative length of stay * 90-day postoperative morbidity

A total of 160 participants will be enrolled. Analysis will be conducted on an intention-to-treat basis.

Вмешательства

  • Другое Standard Jejunostomy Feed (Nutrison Protein Plus)
    Postoperative enteral feeding using a standard long-chain triglyceride-based jejunostomy formula (Nutrison Protein Plus 1.25 kcal/ml), initiated on postoperative day 1 and escalated according to institutional feeding protocol.
  • Другое MCT-Based Jejunostomy Feed (Nutrison Peptisorb)
    Postoperative enteral feeding using a medium-chain triglyceride-based jejunostomy formula (Nutrison Peptisorb 1 kcal/ml), initiated on postoperative day 1 and escalated according to institutional feeding protocol.

Первичные конечные точки

  • Incidence of Clinically and Biochemically Confirmed Chylothorax [Срок оценки: Postoperative days 1,3 and 5]

Критерии участия

Критерии включения

  • Age ≥ 18 years
  • Diagnosis of oesophageal cancer (adenocarcinoma or squamous cell carcinoma)
  • Planned minimally invasive or robotic-assisted oesophagectomy (MIO or RAMIO) with curative intent
  • Placement of feeding jejunostomy at or prior to oesophagectomy
  • Able to provide written informed consent

Критерии исключения

  • Inability to provide informed consent
  • No feeding jejunostomy placed at or prior to surgery
  • Prior or concomitant malignancy that would interfere with study protocol or outcomes

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
Простое слепое
Основная цель
Профилактика

Центры проведения

Ирландия · 1 центр
  • Beaumont RCSI Cancer Centre — Beaumont

Идентификаторы

NCT: NCT07616245 · 25-11

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗