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Market Research - Acceptability Study for New MCT Fat Products

Market Research - Acceptability Study for a Range of New MCT Based Products (Dr Schär - Kanso) Kanso DeliMCT 53% (Cream) Kanso DeliMCT 28% (Tomato or Mushroom) Kanso DeliMCT 21% (Cacaobar)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04309214
Enrollment
12
Registered
2020-03-16
Start date
2018-11-26
Completion date
2019-01-21
Last updated
2020-03-16

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

Conditions

Epilepsy, Fatty Acid Oxidation Disorder, Ketogenic Diet, Ketosis, Malabsorption, Medium Chain Triglycerides

Brief summary

This is a market research, observational study to evaluate the tolerability and acceptability of MCT supplements for young children, young people and adults with intractable epilepsy, GLUT-1 or PDHD from 3 years to adulthood.

Interventions

DIETARY_SUPPLEMENTMCT fats

Subjects will be asked to take 3 new MCT products for 7 days each over a 25 day period

Sponsors

Dr. Schär AG / SPA
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
3 Years to 20 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of epilepsy requiring a ketogenic or a specialist diet as part of their treatment. * Subjects new to taking or who are already taking an MCT product and are willing to try each of the 3 study products for 7 days each. 21 days taking product with 2 days between each new product trialled. * Those patients who have been taking MCT in their diet should do so for a minimum of 4 weeks before commencement of the study. * Patients aged 3 years of age to adulthood. * Written informed consent obtained from patient or parental caregiver.

Exclusion criteria

* Presence of serious concurrent illness * Investigator's uncertainty about the willingness or ability of the patient to comply with the protocol requirements * Participation in any other studies involving investigational or marketed products concomitantly or within two weeks prior to entry into the study * Any patients having taken antibiotics over the previous 2 weeks leading up to the study * Patients already on and MCT product who have been taking it in their diet for less than 4 weeks * Patients less than 3 years of age * Patients over 20 years.

Design outcomes

Primary

MeasureTime frameDescription
Gastrointestinal tolerance7 days for each product, maximum 25 daysQuestionnaire detailing any GI symptoms, severity and change from usual The collection of daily data about the gastrointestinal tolerance of the product
Product compliance7 days for each product, maximum 25 daysDaily questionnaire on amounts offered and amounts actually consumed, compared to recommended amount.
Product palatability7 days for each product, maximum 25 daysQuestionnaire data captured to evaluate taste
Product acceptability7 days for each product, maximum 25 daysBrief tick-box questionnaire on overall liking and acceptability of product

Countries

United Kingdom

Outcome results

None listed

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