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Acceptability and Tolerance Study of a High Energy Tube Feed with Food Derived Ingredients

NCT06034951 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 16

Last updated 2024-09-23

No results posted yet for this study

Summary

Enterally fed adults and children who are assessed by the dietitian as requiring an adult high-energy, fibre-containing enteral formula will be recruited. Data from 15 participants are required in order to submit an application to the Advisory Committee on Borderline Substances (ACBS) for product registration.

Conditions

  • Tolerance

Interventions

DIETARY_SUPPLEMENT

Compleat 1.5 HP

Patients well established and stable on an enteral tube feed. This group will act as their own controls and switched to the new tube feed.

Sponsors & Collaborators

  • Société des Produits Nestlé (SPN)

    lead INDUSTRY

Principal Investigators

  • Martha Van Der Linde · Community Paediatric Dietitian Worcestershire North Nutrition and Dietetic Hastings Way, Worcester. UK

  • Amy Carter · The Walton Centre NHS Foundation Trust, Liverpool UK

  • Sam Ogundere · Lewisham and Greenwich NHS 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
15 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-05-24
Primary Completion
2023-08-21
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 NCT06034951 on ClinicalTrials.gov