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Acceptability and Tolerance Study of Peptide Feed With Fibre

Dietary Exposure Clinical Trial

Official title:
To Evaluate the Acceptability (Including Gastrointestinal Tolerance and Compliance) of an Adult Peptide 1.3 kcal/ml Tube-feed Formula Containing Partially Hydrolysed Guar Gum (PHGG) Fibre.

Clinical Trial Summary

Enterally fed adults with documented evidence of gastrointestinal intolerance will be recruited. Participants will be deemed by the investigator as having a clinical indication for enteral feeding with a fibre containing peptide formula. Data from 15 participants are required in order to submit an application to the Advisory Committee on Borderline Substances (ACBS) for product registration.

Clinical Trial Description

To evaluate the acceptability (including gastrointestinal tolerance and compliance) of an adult enteral peptide formula containing Partially Hydrolysed Guar Gum (PHGG) fibre in 15 patients. This is a single arm, prospective, multi-centre study to evaluate the gastrointestinal tolerance and compliance over a fourteen-day period. Data will be collected using patient diaries to asses changes in GI tolerance and tube feed intake. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06102135
Study type Interventional
Source Société des Produits Nestlé (SPN)
Contact Stephanie Wakefield
Phone 0191 282 3345
Email stephanie.wakefield3@nhs.net
Status Recruiting
Phase N/A
Start date September 5, 2023
Completion date September 21, 2024
View Details
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