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Trial of Enteral Nutrition Enriched With Eicosapentaenoic Acid (EPA) in Upper Gastrointestinal Cancer Surgery

Randomized Double Blinded Trial to Investigate Effects of an Enteral Nutritional Supplement Enriched With Eicosapentaenoic Acid on Body Composition,Complications,Stress Response,Immune Function & Quality of Life in After Esophagectomy

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00790140
Enrollment
120
Registered
2008-11-13
Start date
2005-07-31
Completion date
2010-07-31
Last updated
2008-11-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Esophageal Cancer

Keywords

Esophageal Cancer, esophagectomy, enteral feeding, body composition, immunology

Brief summary

This study aims to examine whether providing tube feeding with a formula enriched with omega-3 fats is better than traditional standard tube feeding in terms of preserving nutritional status, improving immune function and reducing medical complications following major upper Gut cancer surgery.

Detailed description

Title A double blinded randomized controlled trial to investigate the effects of an enteral nutritional supplement enriched with Eicosapentaenoic acid on long term nutritional status post operatively specifically the maintenance of lean body mass, and its potential impact on quality of life as well as examining the stress response and immune function and in patients undergoing surgical treatment of esophageal cancer. Investigational medicinal Product(s): Prosure (Abbott Laboratories) Comparator: Ensure Plus (Abbott Laboratories) Study Objectives To examine whether prolonged supplementation with a nutritional supplement enriched with Eicosapentaenoic acid is superior to standard nutritional products in terms of promoting anabolism and improving quality of life in patients undergoing surgical treatment of esophageal cancer. Study Design - Prospective randomized controlled trial. Primary Endpoints: * Quality of life Scores using EORTC Questionnaires * Nutritional status on day 21 post oesophagectomy and/or total gastrectomy(specifically lean body mass) and at out patient follow up Secondary Endpoints: * Effects on the immuno-inflammatory response to surgery * Post operative Clinical outcome including SIRS, sepsis and organ failure

Interventions

DIETARY_SUPPLEMENTProsure

This is an enteral tube feed with 125 kcals & 6.65g protein per 100mls. It contains Fat, Carbohydrate, and vitamins and minerals and is enriched with 2.2g Eicosapentaenoic Acid per 500mls of feed. Patients on this trial who are randomized to Prosure will receive the product orally for 5 days prior to surgery and for 21 days post surgery vis a feeding jejunostomy tube

DIETARY_SUPPLEMENTEnsure Plus

This is a standard enteral tube feed with 150 kcals & 6.3 g protein per 100mls as well as carbohydrate, fat and vitamins and minerals. It does not have any active immunonutrients. Patients randomized to this arm will receive the product for 5 days pre op and 21 days post surgery via a feeding jejunostomy tube

Sponsors

Abbott
CollaboratorINDUSTRY
University of Dublin, Trinity College
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Adult (male & female) patients \>18 years with resectable esophageal cancer

Exclusion criteria

* Patients with metastatic disease, * Non-operable cases, * Patients requiring chemotherapy/radiotherapy early following surgery, * Patients with known immunological disorder, * Emergency esophagectomy cases, * Patients with cardiac, liver or renal failure, * Active small intestinal disease eg Crohns disease, * Allergy to any of the ingredients, * Uncontrollable Diabetes, * Use of medications known to affect eicosanoid metabolism in two weeks prior to trial, * Use of fish oil/n-3 fatty acids, * Drug Abuse, * Unable to take preparation for 5 days preoperatively, * Pregnant women, * Cessation of enteral feeding for longer than 3 consecutive days post operatively for medical/surgical reasons (e.g. Chyle leaks).

Design outcomes

Primary

MeasureTime frame
Preservation of body compostition after surgery2 months

Secondary

MeasureTime frame
Reduced immuno-inflammatory response to surgery2 months

Countries

Ireland

Contacts

Primary ContactAoife Ryan, PhD
ryana1@tcd.ie+35314284452
Backup ContactJohn V Reynolds, MD
reynoldsjv@stjames.ie+35314162211

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026