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Acceptability and Tolerance Study of Adult Tube Feed With Food With Food Derived Ingredients.

Dietary Exposure Clinical Trial

Official title:
To Evaluate the Acceptability (Including Gastrointestinal Tolerance and Compliance) of an Adult Tube-feed Formula With Ingredients Derived From Food.

Clinical Trial Summary

Product acceptability data from 15 participants are required in order to submit an application to the Advisory Committee on Borderline Substances (ACBS) and the Health Service Executive (HSE) submission for Ireland for product registration.

Clinical Trial Description

To evaluate the acceptability (including gastrointestinal tolerance and compliance) of an adult tube-feed formula with ingredients derived from food for the dietary management of participants who require a tube feed. . The acceptability data from 15 participants will be collected in order to submit an application to the Advisory Committee on Borderline Substances (ACBS) and the Health Service Executive (HSE) for Ireland. Participants will be provided with one month supply of tube feed and will be asked to complete a daily diary and short questionnaire to record information allowing assessment of the following: - Gastrointestinal tolerance - Compliance with prescribed feed volumes ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06102122
Study type Interventional
Source Société des Produits Nestlé (SPN)
Contact
Status Completed
Phase N/A
Start date August 22, 2023
Completion date December 22, 2023
View Details
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