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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ISRCTN |
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Last refreshed on:
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2 September 2019 |
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Main ID: |
ISRCTN13406789 |
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Date of registration:
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16/02/2018 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Postprandial cheese matrix study
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Scientific title:
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Post-prandial randomised controlled trial to examine the postprandial effects of dairy fat within different matrices |
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Date of first enrolment:
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01/02/2018 |
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Target sample size:
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10 |
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Recruitment status: |
Completed |
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URL:
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http://isrctn.com/ISRCTN13406789 |
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Study type:
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Interventional |
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Study design:
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Single-centre randomised cross-over intervention trial (Other)
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Phase:
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Not Applicable
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Countries of recruitment
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Ireland
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Contacts
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Name:
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Emma
Feeney |
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Address:
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UCD Centre for Molecular Innovation and Drug Discovery
Science Centre South, Belfield
D04 V1 W8
Dublin
Ireland |
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Telephone:
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Email:
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Affiliation:
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Name:
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Address:
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Key inclusion & exclusion criteria
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Inclusion criteria:
1. Fasting triglycerides <2.5
2. BMI 18-35
Exclusion criteria:
1. Familial hypercholesteraemia
2. Fasting triglycerides greater than 2.5
3. Any diagnosed metabolic disorder such as diabetes type 1 or 2
Age minimum:
Age maximum:
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Blood lipids
Nutritional, Metabolic, Endocrine
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Intervention(s)
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Subjects will receive three meals which contain dairy fat in varying levels of a cheese matrix, with a slice of toast as a carrier, in a random order with a 5-7 day washout period in between meals. Due to the nature of the meals, the arms cannot be masked.
Arm 1: 120g full fat cheddar cheese and a slice of low-fibre white toast
Arm 2: 120g reduced fat cheddar cheese and a slice of low-fibre white toast
Arm 3: 30g calcium caseinate powder
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Primary Outcome(s)
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Circulating fatty acids measured with a Randox Daytona from blood samples collected at fasting, and hourly, on the hour, for the 6-hour postprandial period
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Secondary Outcome(s)
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Blood glucose measured with a Randox Daytona from blood samples collected at fasting, and hourly for the 6-hour post-prandial period
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Secondary ID(s)
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LS-17-103
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Source(s) of Monetary Support
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Enterprise Ireland
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Ethics review
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Status:
Approval date:
Contact:
Human Research Ethics Committee in University College Dublin, 24/01/2018, ref. LS-17-103
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Results
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Results available:
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Yes |
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Date Posted:
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Date Completed:
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31/08/2018 |
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URL:
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