Trials Sponsors Conditions Drugs Pricing

Conditions

Disease Related Malnutrition

Outcome Measures

Primary Outcomes (3)

Gastrointestinal tolerance
Participants record gastrointestinal symptoms each day in a diary: nausea, vomiting, bloating, abdominal pain, constipation, diarrhoea, and burping or flatulence. Each symptom is rated none, mild, moderate or severe. Bowel movement frequency and stool type are recorded each day using the Bristol Stool Chart. Results are reported as how often each symptom occurs and how severe it is, compared with symptoms recorded at baseline.
Baseline and daily from Day 1 to Day 7
Compliance with the prescribed oral nutritional supplement
Participants record each day in a diary the number of servings prescribed and taken, and the reasons for any missed or partly taken servings. Compliance is reported as the percentage of prescribed servings each participant took over the study period.
Daily from Day 1 to Day 7
Palatability of the oral nutritional supplement
Participants complete a questionnaire rating appearance, smell, taste, texture, aftertaste, convenience and how pleasant the supplement is to take. Each item is scored on a 5-point Likert scale from 1 (strongly disagree) to 5 (strongly agree). Overall satisfaction is rated on a 5-point scale from 1 (very dissatisfied) to 5 (very satisfied).
Day 7

Secondary Outcomes (1)

Adverse events
Day 1 to Day 7

Study Arms (1)

Oral nutritional supplement

EXPERIMENTAL

All participants take the oral nutritional supplement every day for 7 days, at one or two servings a day as prescribed by the study dietitian. Participants record their intake and any stomach or bowel symptoms in a daily diary, and complete a questionnaire and a review with the study team on Day 7.

Dietary Supplement: Oral nutritional supplementation

Interventions

Oral nutritional supplementationDietary supplement

A Food for Special Medical Purposes taken orally, one or two servings a day as prescribed by the study dietitian, for 7 days.

Oral nutritional supplement

Eligibility Criteria

Age18 Years+

Sexall

Healthy VolunteersNo

Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

Aged 18 years or over
Male or female

Sponsors & Collaborators

Aymes International Limited
Industrylead

Study Sites (1)

Nottingham University Hospitals NHS Trust

Nottingham, NG7 2UH, United Kingdom

Alison Head of Research Governance and QualityCONTACT0115 924 9924 ext. 80755 nuhnt.researchsponsor@nhs.net

MeSH Terms

Interventions

Dietary Supplements

Intervention Hierarchy (Ancestors)

FoodDiet, Food, and NutritionPhysiological PhenomenaFood and Beverages

Study Design

Study Type: interventional
Phase: not applicable
Allocation: NA
Masking: NONE
Purpose: OTHER
Intervention Model: SINGLE GROUP
Sponsor Type: INDUSTRY
Responsible Party: SPONSOR

Study Record Dates

First Submitted

October 23, 2026

First Posted

October 29, 2026

Study Start

November 2026

Estimated

Planned date reported by the registry; this milestone is not confirmed as achieved.

Primary Completion

December 2026

Estimated

Tolerance and Acceptability of an Oral Nutrition Supplement

Brief Summary

Registry Overview

Trial Relationships

Study Timeline

First Submitted

First Posted

Study Start

Primary Completion

Study Completion

Conditions

Outcome Measures

Primary Outcomes (3)

Secondary Outcomes (1)

Study Arms (1)

Oral nutritional supplement

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Interventions

Intervention Hierarchy (Ancestors)

Study Design

Study Record Dates

You may not qualify if:

Data Sharing

Source record

Locations

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

First Submitted

First Posted

Study Start

Primary Completion

Study Completion

Conditions

Outcome Measures

Primary Outcomes (3)

Secondary Outcomes (1)

Study Arms (1)

Oral nutritional supplement

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Interventions

Intervention Hierarchy (Ancestors)

Study Design

Study Record Dates

You may not qualify if:

Data Sharing

Source record

Locations