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Clinical Trials in Ireland / NCT07616245
Recruiting Not applicable

MCT Enteral Feeding to Reduce Chyle Leak After Oesophagectomy

NCT07616245 · tracked via the Priya Life Science Ireland tracker
Sponsor
Royal College of Surgeons, Ireland
Phase
Not applicable
Started
2025-10-02
Last updated
2026-06-01

Condition(s) studied

Oesphageal Cancer

Investigational drug(s) / intervention(s)

Standard Jejunostomy Feed (Nutrison Protein Plus)MCT-Based Jejunostomy Feed (Nutrison Peptisorb)

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.

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.

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * 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 Exclusion Criteria: * 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

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Beaumont RCSI Cancer Centre Beaumont Dublin Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07616245 on ClinicalTrials.gov ↗ ← All trials in Ireland