TOLERANCE AND ACCEPTABILITY EVALUATION OF AYMES 'OSLO'
Research type
Research Study
Full title
TOLERANCE AND ACCEPTABILITY EVALUATION OF AYMES 'OSLO'
IRAS ID
213057
Contact name
Carole Springett
Contact email
Duration of Study in the UK
0 years, 0 months, 15 days
Research summary
The purpose of this study is to investigate the tolerance (bowel movements / Gastro-Intestinal (GI) side effects) and acceptability (sensory qualities/volume) of AYMES OSLO (a high energy oral nutritional supplement (ONS)) in patients requiring supplementary oral nutritional support compared with currently available ONS. It is of relevance to patients, health care professionals (HCP) and the general public as it provides data which can be submitted to the Advisory Committee on Borderline Substances (ACBS). The ACBS is the governing body that makes the decision whether or not an ONS can be prescribed in the community at the expense of the NHS.
REC name
London - Surrey Research Ethics Committee
REC reference
16/LO/1643
Date of REC Opinion
13 Oct 2016
REC opinion
Further Information Favourable Opinion