Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07417514

Tolerance and Acceptability Evaluation of an Oral Nutrition Supplement

Led by Aymes International Limited · Updated on 2026-02-18

40

Participants Needed

1

Research Sites

182 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

To evaluate the tolerance (gastrointestinal) and acceptability of a new Oral Nutrition Supplement in patients with or at risk of disease related malnutrition, taken either orally or via a feeding tube

CONDITIONS

Official Title

Tolerance and Acceptability Evaluation of an Oral Nutrition Supplement

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients (≥18 years) who are able to communicate clearly
  • Diagnosis of renal disease or confirmed need for protein supplementation by a qualified healthcare professional
  • Patients with or at risk of malnutrition as determined by nutritional screening tools or clinical judgement
  • Expected to require an oral nutrition supplement for at least 28 days, able to take flavor variants orally and neutral variant via feeding tube
  • Informed consent obtained
Not Eligible

You will not qualify if you...

  • Participation in other studies involving investigational or marketed products within 7 days prior to this study
  • Medical or dietary contraindication to any ingredients in the supplement
  • No feeding tube for patients taking the neutral variant
  • Significant liver impairment
  • Dysphagia requiring IDDSI level 1 or higher fluids
  • Uncontrolled inflammatory bowel disease or prior bowel resection with ongoing symptoms
  • Use of antibiotics in the 2 weeks before the study
  • Unable to give informed consent, including patients with dementia
  • Under 18 years of age
  • Insufficient proficiency in English language
  • Investigator doubts about patient’s willingness or ability to follow study protocol

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

UCLH NHS Foundation Trust

London, United Kingdom, NW1 2PG

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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