Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
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
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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