Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06288464

Does Distal Enteral Feeding of Fibre Positively Affect the Microflora in the Distal Limb of Loop Ileostomy Patients?

Led by Lancashire Teaching Hospitals NHS Foundation Trust · Updated on 2025-04-06

15

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

L

Lancashire Teaching Hospitals NHS Foundation Trust

Lead Sponsor

L

Lancaster University

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research focuses on patients who have had a diseased section of their bowel surgically removed and often require a temporary stoma to divert bowel contents while the remaining bowel heals. The study explores whether replenishing the beneficial bacteria in the non-functioning section of the bowel before reversal surgery can reduce complications such as inflammation or poor bowel function, which affect many patients and sometimes prevent reversal surgery altogether. The study involves delivering a nutritional supplement called Ensure17, which contains amino acids, vitamins, and minerals, through a feeding tube into the defunctioned bowel segment for about four weeks. During the last 7 to 14 days of this feeding, a soluble fibre made from chicory root extract will be added to the nutrition to support the growth of healthy bacteria. This feeding method aims to improve the health of the bowel tissue and its microflora before the bowel is rejoined. Participants will be monitored through various tests to measure changes in the types and amounts of bacteria and immune cells in the bowel, as well as tissue health. Researchers will also track hospital stay length and the rate of postoperative complications during the study period. The overall participation lasts around one month, during which patients are carefully observed to assess the effects of the fibre supplementation on bowel recovery.

CONDITIONS

Brief Title

Enteral Feeding of Fibre to Improve Microbiota

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Any individual identified for distal (stoma) feeding who can understand verbal and written English to provide informed consent
  • Participants undergoing ileostomy or colostomy reversal surgery
Not Eligible

You will not qualify if you...

  • Not undergoing ileostomy or colostomy reversal
  • Unable to understand verbal explanations or written information given in English

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - Approximately 4 weeks

Participants receive enteral feeding through a stoma feeding tube for approximately 4 weeks. For the final 7 to 14 days, 10g of soluble fibre is added daily to the nutritional supplement fed into the stoma.

Daily feeding through stoma tube

Trial Site Locations

Total: 1 location

1

Lancashire Teaching Hospitals NHS

Preston, Lancashire, United Kingdom, PR2 9HT

Actively Recruiting

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Research Team

K

Kina Bennett

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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