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Clinical Trial Summary

Required for Advisory Committee for Borderline Substances (ACBS) approval. Aim of this study is to access the palatability, compliance and GI-tolerance of Nutricomp® Drink Plus to show that it is acceptable for patients in the United Kingdom.


Clinical Trial Description

n/a


Study Design

Intervention Model: Single Group Assignment, Masking: Open Label


Related Conditions & MeSH terms


NCT number NCT02538250
Study type Interventional
Source B. Braun Melsungen AG
Contact
Status Completed
Phase Phase 4
Start date July 2015
Completion date October 2015

See also
  Status Clinical Trial Phase
Completed NCT03588169 - Representations of Oral Nutritional Supplementation (ONS) in Hospitals : Gender differences_observational Study