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Acceptability (Including Gastrointestinal Tolerance and Compliance) of a Paediatric and Adult Bolus Tube Feed With Food Blends
This is a prospective acceptability study to evaluate the gastrointestinal tolerance and compliance of a bolus tube feed over a 28 -day period for up to 50 participants. The enteral bolus formula is for the dietary management of patients with short bowel syndrome; intractable malabsorption; preoperative preparation of undernourished patients; inflammatory bowel disease; total gastrectomy; dysphagia; bowel fistulae; feeding intolerances, developmental disabilities, and disease related malnutrition.
The study will collect data in 50 children and adults over a period of 28 days. Gastrointestinal tolerance will be collected over 7 days and formula intake will be over 28 days. A patient satisfaction questionnaire will be completed at the end of the study.
Age
1 - No limit years
Sex
ALL
Healthy Volunteers
No
Queen Medical Hospital Nutrition and Dietetics
Nottingham, United Kingdom
Dietetic Team 1st floor Kings Court 1, Charles Hastings Way,
Worcester, United Kingdom
Start Date
December 10, 2025
Primary Completion Date
November 10, 2026
Completion Date
November 11, 2026
Last Updated
January 14, 2026
50
ESTIMATED participants
Tube feed
DIETARY_SUPPLEMENT
Sarah Durnan, PHD, BSc Nutrition Dietetics
CONTACT
Lead Sponsor
Société des Produits Nestlé (SPN)
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06868524