Trials / Completed
CompletedNCT02831647
Acceptability and Tolerance Study of New Oral Nutritional Supplement PRAGUE
Tolerance and Acceptability of AYMES PRAGUE
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 20 (actual)
- Sponsor
- Aymes International Limited · Industry
- Sex
- All
- Age
- 18 Years – 100 Years
- Healthy volunteers
- Not accepted
Summary
Tolerance and Acceptability of new oral nutritional supplement - AYMES PRAGUE
Detailed description
To evaluate tolerance and acceptability of AYMES PRAGUE in patients requiring supplementary oral nutritional support compared with currently available alternatives, measuring outcomes of GI effects, Compliance, product preference,convenience etc. To obtain data to support an ACBS submissions for AYMES PRAGUE (to allow for prescription in the community at NHS expense).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | AYMES PRAGUE | AYMES PRAGUE is a ready to drink, high energy, low volume oral nutritional supplement drink. It provides 300 kcal and 12g protein per 125ml serving. It is a Food for Special Medical Purposes (FSMP) and must therefore be used under medical supervision. It is not designed as a sole source of nutrition. |
Timeline
- Start date
- 2016-09-01
- Primary completion
- 2016-12-01
- Completion
- 2016-12-01
- First posted
- 2016-07-13
- Last updated
- 2020-01-09
Source: ClinicalTrials.gov record NCT02831647. Inclusion in this directory is not an endorsement.