Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12611000740998
Ethics application status
Approved
Date submitted
13/07/2011
Date registered
14/07/2011
Date last updated
5/02/2020
Date data sharing statement initially provided
5/02/2020
Date results provided
5/02/2020
Type of registration
Prospectively registered

Titles & IDs
Public title
Comparative effects of A1 versus A2 milk on gastrointestinal symptoms and systemic exposure to beta-casomorphin-7 (BCM7)
Scientific title
Adults and the effect of A1 versus A2 milk consumption on gastrointestinal symptoms and systemic exposure to beta-casomorphin-7 (BCM7)
Secondary ID [1] 262621 0
Nil
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Gastrointestinal symptoms related to milk intolerance 268317 0
Condition category
Condition code
Oral and Gastrointestinal 268448 268448 0 0
Normal oral and gastrointestinal development and function
Diet and Nutrition 268455 268455 0 0
Other diet and nutrition disorders

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
This will be a randomised, crossover study over an 8 week period consisting of 2 weeks of an initial washout. Following washout, 40 participants will be randomised to either the A1 milk or A2 milk group (Crossover 1), with 20 in each group. This is then followed by another 2 weeks washout after which Subjects will then start the alternative A1 or A2 milk Intervention for another 2 weeks intervention (crossover2).

During washout, participants will consume their normal diet (excluding all dairy) and use rice milk and rice yoghurt alternatives to replace habitual daily dairy intake.

Intervention consists of either:
1) a normal diet (excluding all dairy) + 750mL A2 beta-casein protein containing milk consumed in 3 serves daily (~7-8g A2 type beta-casein/day)
or
2) Normal diet (excluding all dairy) + 750mL A1 containing milk per day, which is equivalent to ~7-8g A1 type beta-casein/day;

Milk will be given as UHT long life, skim milk (A2 Dairy Products Australia)
Average composition:
energy 189kJ/100mL
total protein 3.1g/100mL
total fat 0.1g/100mL
carbohydrate (including lactose) 5.2g/100mL
Intervention code [1] 266968 0
Treatment: Other
Comparator / control treatment
Normal diet (excluding all dairy) + 750mL A1 beta-casein protein containing milk consumed in 3 serves daily (~7-8g A1 type beta-casein/day) for 2 weeks. Milk will be given as UHT long life, reduced fat milk (A2 Dairy Products Australia) Average composition: energy 189kJ/100mL total protein 3.1g/100mL total fat 2.5g/100mL carbohydrate (including lactose) 5.2g/100mL
Control group
Active

Outcomes
Primary outcome [1] 269204 0
Gastrointestinal symptom management.
Participants will record gastrointestinal symptoms of intolerance in their Symptom Report Diary and daily bowel movement frequency/stool consistency using the Bristol Stool Scale.
Timepoint [1] 269204 0
Symptoms recorded during each 2 week intervention period
Secondary outcome [1] 279113 0
Investigation of the presence of BCM-7 in serum from fasting and postprandial blood samples
Timepoint [1] 279113 0
At the beginning and end of each 2 week intervention period
1 hour postprandial sample after consumption of 500mL of milk intervention at the end of each 2 week intervention period
Secondary outcome [2] 279114 0
Measurement of gastrointestinal tract permeability from a dual sugar test and urine analysis
Timepoint [2] 279114 0
At the end of each 2 week intervention period
Secondary outcome [3] 279138 0
Measurement of gut inflammation from analysis of faecal calprotectin to investigate possible precursors to BCM-7 effects
Timepoint [3] 279138 0
At the end of each 2 week intervention period

Eligibility
Key inclusion criteria
Caucasian
Do not drink more than 1 serve milk/day
Those who report lactose intolerance but have not received medial diagnosis
Willing to consume milk for 8 weeks
Able to sign and understand informed consent
Minimum age
18 Years
Maximum age
65 Years
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
Milk allergy
Diagnosed lactose intolerance
Pregnancy and lactation
Cardiovascular event in the last 6 months
Current, habitual opioid consumption
Antibiotic treatment within the last 8 weeks prior to screening
Immunosuppressive medications or anti-inflammatory drugs within the last 4 weeks prior to screening

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Potential participants will be screened and attend a briefing session to assess suitability. Suitable participants will be allocated to a group by central randomisation by computer
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computer program generated randomisation plan
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?



Intervention assignment
Crossover
Other design features
Phase
Not Applicable
Type of endpoint/s
Efficacy
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
1/09/2011
Actual
13/02/2012
Date of last participant enrolment
Anticipated
Actual
14/06/2012
Date of last data collection
Anticipated
Actual
17/08/2012
Sample size
Target
40
Accrual to date
Final
41
Recruitment in Australia
Recruitment state(s)
WA

Funding & Sponsors
Funding source category [1] 267447 0
Commercial sector/Industry
Name [1] 267447 0
A2 Dairy Products Australia
Country [1] 267447 0
Australia
Primary sponsor type
University
Name
Curtin University of Technology
Address
GPO Box U1987
Perth, Western Australia 6845
Country
Australia
Secondary sponsor category [1] 266489 0
None
Name [1] 266489 0
Address [1] 266489 0
Country [1] 266489 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 269414 0
Curtin University Human Ethics Committee
Ethics committee address [1] 269414 0
Ethics committee country [1] 269414 0
Australia
Date submitted for ethics approval [1] 269414 0
15/07/2011
Approval date [1] 269414 0
04/10/2011
Ethics approval number [1] 269414 0
HR102/2011

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 32870 0
A/Prof Sebely Pal
Address 32870 0
School of Public Health Curtin University GPO Box U1987 Perth WA 6845
Country 32870 0
Australia
Phone 32870 0
+61 8 9266 4755
Fax 32870 0
Email 32870 0
[email protected]
Contact person for public queries
Name 16117 0
Assoc Prof Sebely Pal
Address 16117 0
School of Public Health
Curtin University
GPO Box U1987
Perth WA 6845
Country 16117 0
Australia
Phone 16117 0
+61 8 9266 4755
Fax 16117 0
Email 16117 0
[email protected]
Contact person for scientific queries
Name 7045 0
Assoc Prof Sebely Pal
Address 7045 0
School of Public Health
Curtin University
GPO Box U1987
Perth WA 6845
Country 7045 0
Australia
Phone 7045 0
+61 8 9266 4755
Fax 7045 0
Email 7045 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment
Data sharing was not part of the planning for this project


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.