Tolerance
Conditions
Brief summary
Enterally fed adults and children who are assessed by the dietitian as requiring an adult high-energy, fibre-containing enteral formula will be recruited. Data from 15 participants are required in order to submit an application to the Advisory Committee on Borderline Substances (ACBS) for product registration.
Detailed description
To evaluate the acceptability (including gastrointestinal tolerance and compliance) of a high energy, adult enteral formula with food-derived ingredients.This is a single arm, prospective, multi-centre study to evaluate the gastrointestinal tolerance and compliance over a 14-day period with the new tube feed. Participants or their caregivers will be provided with 14-day supply of the new tube feed and will be asked to complete a daily diary and short questionnaire to record information allowing assessment of the following: * Gastrointestinal tolerance * Compliance with prescribed feed volume
Interventions
DIETARY_SUPPLEMENTCompleat 1.5 HP
Patients well established and stable on an enteral tube feed. This group will act as their own controls and switched to the new tube feed.
Sponsors
Société des Produits Nestlé (SPN)
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
15 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patients requiring an enteral tube feed (taking \> 60% of energy needs from their feeding tube) as part of their dietary management for disease related malnutrition * Children 15 years and over * Adults and children requiring an adult high-energy and fibre-containing formula, as assessed by the dietitian. * Patients well-established and stable on enteral feeding. * Willingly given, written, informed consent from patient or consultee * Willingly given, written assent (if appropriate).
Exclusion criteria
* Inability to comply with the study protocol, in the opinion of the investigator * Children under 15 years of age * Patients receiving mechanical ventilation, sedation or inotropic support * Patients on total parenteral nutrition * Known food allergies to any ingredients (see ingredients list) or galactosaemia * Patients with significant renal or hepatic impairment * Patients with planned changes to medication or treatments during the study period which may alter gastrointestinal function (e.g. chemotherapy). Changes in medications or nutritional products during the study intervention must be documented. * Participation in another interventional study within 2 weeks of this study. * Patients with a clinical indication for a low fibre or fibre free diet as advised by the healthcare team. * Patients with known or suspected ileus or mechanical bowel obstruction
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Daily formula intake | 14 days | mL per day |
| Daily patient diaries | 14 days | Daily monitor of gastrointestinal tolerance using questionnaire on increase, decrease or no change |
Countries
United Kingdom
Outcome results
None listed