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A Study to Evaluate the Palatability of a Nutritional Support Biscuit (Fitabisc)

A Study to Evaluate the Palatability of a Nutritional Support Biscuit (Fitabisc)

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03859661
Acronym
Fitabisc
Enrollment
10
Registered
2019-03-01
Start date
2015-12-31
Completion date
2017-09-11
Last updated
2019-03-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Surgery

Brief summary

A study to evaluate the palatability of a nutritional support biscuit (Fitabisc) in patients about to undergo colorectal surgery.

Detailed description

The question of preoperative supplementation raises another issue about how this might be provided for patients, especially at home. The Chief Investigator has formulated a new biscuit 'Fitabisc' that contains the key antioxidants; vitamins C and E, selenium and glutamine. The advantage of a biscuit is that all ingredients of interest are combined within the one item and so this may be easier for patients to 'take' than other types of supplement. A survey involving 17 community pharmacies in England and Northern Ireland found that 60% of patients aged 60 - 89 years had difficulty swallowing tablets and capsules. The consistency of the biscuit is softer than traditional shortbread and crumbs readily which we hope will make it easy to eat. The aim of this study is to test the palatability of Fitabisc and whether patients undergoing abdominal surgery can eat it in the desired quantities for 10 days before they are admitted to hospital. In summary, most studies to date have looked perioperative or postoperative supplementation with antioxidants alone. No attempt has been made to do this using a palatable biscuit that would facilitate preoperative oral supplementation. If this study confirms the palatability of the biscuit and there is adherence to eating it then it would be our intention to set up a prospective randomized study in which the potential efficacy of Fitabisc would be evaluated.

Interventions

DIETARY_SUPPLEMENTFitabisc

Fitabisc is a chocolate cookie with vanilla cream filling which contains the most important antioxidants Vitamin C, Vitamin E, and the mineral Selenium. Fitabisc is not commercially available and for the purposes of this study it will be manufactured by Calerrific Ltd, which already produces a biscuit called CalBisc 100 as a simple calorie and nutritional supplement. Production takes place in a BRC Global Standard Grade A certified bakery operated by Farringford Foods in Portadown, Northern Ireland.

Sponsors

York Teaching Hospitals NHS Foundation Trust
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
16 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients between the ages of 16 and 80 years inclusive. * Patients who are having colorectal surgery. * Patients who are able to give voluntary, written informed consent to participate in the study and from whom written consent has been obtained.

Exclusion criteria

* Those who cannot or do not provide informed consent * Patients with a known or suspected allergy to any of the ingredients of Fitabisc e.g. gluten or dairy products * Patients with one of the following co-morbidities: * Haemochromatosis * Thalassaemia * Kidney disease * Liver disease * Reye syndrome * Patients who already take supplements of vitamin C, E, selenium or glutamine. * Patients with type 1 diabetes, or type 2 diabetes that requires them to have insulin or a hypoglycaemic drug such as Metformin.

Design outcomes

Primary

MeasureTime frameDescription
Adherence to dose10 daysPatients to keep a diary of their consumption
Palatability of biscuit10 daysStudy will measure palatability on a standard Likert scale after 10 days

Secondary

MeasureTime frameDescription
Progress of patients following surgery4-6 weeks post op.Adverse event collection - via patient reported outcomes and review of patient notes following surgery
Collection of events that might be associated with the ingredients of the biscuit.4-6 weeks post op.Adverse event collection - via patient reported outcomes and review of patient notes following surgery

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026