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

NCT06102122 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 18

Last updated 2024-09-23

No results posted yet for this study

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.

Conditions

  • Dietary Exposure

Interventions

DIETARY_SUPPLEMENT

Compleat

Patients well established and stable on a standard enteral tube feed with food derived ingredients will act as their own controls and make a product switch

Sponsors & Collaborators

  • Société des Produits Nestlé (SPN)

    lead INDUSTRY

Principal Investigators

  • Tanita Flood · Royal Hospital for Neuro-disability

  • Martha Van der Linde · Community Paediatric Dietitian Worcestershire, Hastings UK

  • Minal Patel · Barts and London Hospital Trust London UK

  • Adrian Gilson · Newham General Hospital London UK

Study Design

Allocation
NA
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
16 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-08-22
Primary Completion
2023-09-15
Completion
2023-12-22

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06102122 on ClinicalTrials.gov