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Trial registered on ANZCTR
Registration number
ACTRN12608000047392
Ethics application status
Approved
Date submitted
16/01/2008
Date registered
29/01/2008
Date last updated
22/05/2010
Type of registration
Prospectively registered
Titles & IDs
Public title
Growth and nutritional status of infants fed formula based on goat milk or cow milk.
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Scientific title
A randomised trial to compare growth rates and nutritional status of infants fed formula based on goat milk or cow milk
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Secondary ID [1]
508
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G1.071
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Universal Trial Number (UTN)
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Trial acronym
TIGGA
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Infant nutrition
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Condition category
Condition code
Diet and Nutrition
2817
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0
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Other diet and nutrition disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Goat milk infant formula as the sole source of nutrient from enrollment until at least 4 months of age, thereafter with other complementary food up to 12 months of age. The study infant formula will be supplied in cans with appropriate sized scoops to measure the quantity of powder required to make up each feed (12.65g of goat milk powder per 100 ml of formula). The volume and frequency of formula feeding will be specfied by the infants' primary care provider according to the standardised infant feeding guidelines.
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Intervention code [1]
2434
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Other interventions
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Comparator / control treatment
1. Cow milk infant formula as the sole source of nutrient from enrollment until at least 4 months of age, thereafter with other complementary food up to 12 months of age. The cow milk infant formula will be supplied in cans with appropriate sized scoops to measure the quantity of powder required to make up each feed (12.65g of cow milk powder per 100 ml of formula). The volume and frequency of formula feeding will be specfied by the infants' primary care provider according to the standardised infant feeding guidelines
2. Breast milk as the sole source of nutrient from enrollment until at least 4 months of age, thereafter with other complementary food up to 12 months of age.
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Control group
Active
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Outcomes
Primary outcome [1]
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Growth including weight and length. Weight will be measured using electronic scales with baby weighing trays and an error of 5g. A Harpenden Neonatometer will be used for measuring the length of the infants.
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Assessment method [1]
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Timepoint [1]
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at 1, 2, 3, 4, 6 and 12 months of age
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Secondary outcome [1]
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Gastrointestinal tolerance will be assessed by maternal report of frequency and consistency of stool (using The Bristol Stool Form Scale).
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Assessment method [1]
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Timepoint [1]
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at 1, 2, 3 and 4 months of age
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Secondary outcome [2]
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Blood biochemistry will be measured by NATA accredited pathology laboratories
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Assessment method [2]
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Timepoint [2]
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at 4 months of age
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Eligibility
Key inclusion criteria
healthy term infants, birth weight >=2.5kg & <=4.75kg, mother is exclusively feeding an infant formula within 2 weeks of birth or plans to exclusively breastfeed for at least 4 months.
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Minimum age
No limit
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Maximum age
14
Days
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
severe congenital or metabolic disease likely to affect infant feeding or growth, multiple birth.
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Study design
Purpose of the study
Educational / counselling / training
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
central randomisation by phone
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computerised sequence generation. Stratified allocation by gender and study centre. the
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
A parallel breastfed reference group consisting of 100 infants of mothers who plan to exclusively breastfed for at least 4 months will be recruited. mother will be encouraged to continue exclusively breast feeding until 6 months.
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Phase
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Type of endpoint/s
Safety/efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/02/2008
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
300
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
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Commercial sector/Industry
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Name [1]
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Dairy Goat Co-operative (NZ) Ltd
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Address [1]
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18 Gallagher Drive, PO Box 1398,
Hamilton, 3240, NZ
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Country [1]
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New Zealand
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Primary sponsor type
Commercial sector/Industry
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Name
Dairy Goat Co-operative (NZ) Ltd
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Address
18 Gallagher Drive, PO Box 1398,
Hamilton, 3240, NZ
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Country
New Zealand
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Secondary sponsor category [1]
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Other
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Name [1]
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Women's & Children's Health Research Institute
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Address [1]
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72 King William Road
North Adelaide, SA 5006
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Country [1]
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Children, Youth and Women's Health Service
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Ethics committee address [1]
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72 King William Road North Adelaide, SA 5006
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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Approval date [1]
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14/12/2007
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Ethics approval number [1]
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1980/08/10
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Ethics committee name [2]
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Flinders Clinical Research Ethics Committee
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Ethics committee address [2]
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FMC, Level 2, Room 2A221 Bedford Park, SA 5042
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Ethics committee country [2]
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Australia
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Date submitted for ethics approval [2]
4892
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Approval date [2]
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15/11/2007
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Ethics approval number [2]
4892
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25/07
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Summary
Brief summary
This project will compare the growth rates and nutritional status of infants who are exclusively fed formulae either based on goat milk or cow milk. Growth will be assessed regularly (2 weeks, 1, 2, 3, 4, 6 and 12 months). Blood biochemical profile of infants, including plasma amino acids, will be assessed at 4 months. Formula tolerance and stool frequency will be assessed through to 4 months of age and stool microbiota will be assessed through to 2 months of age. A gold standard reference group of breastfed infants will also be included.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Dr Jo Zhou
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Address
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Child Nutrition Research Centre
Women's & Children's Hospital,
72 King William Rd,
North Adelaide, SA 5006
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Country
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Australia
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Phone
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08 8303 4111
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Fax
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08 8303 7135
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Email
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[email protected]
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Contact person for scientific queries
Name
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A/Prof Maria Makrides
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Address
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Women's & Children's Hospital,
72 King William Rd,
North Adelaide, SA 5006
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Country
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Australia
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Phone
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08 8161 6067
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Fax
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08 8161 8228
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Email
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[email protected]
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No information has been provided regarding IPD availability
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
Source
Title
Year of Publication
DOI
Dimensions AI
Nutritional adequacy of goat milk infant formulas for term infants: a double-blind randomised controlled trial
2014
https://doi.org/10.1017/s0007114513004212
Embase
Dietary effects on plasma glycerophospholipids.
2015
https://dx.doi.org/10.1097/MPG.0000000000000783
Embase
Differentiation of bifidobacterium longum subspecies longum and infantis by quantitative PCR using functional gene targets.
2017
https://dx.doi.org/10.7717/peerj.3375
N.B. These documents automatically identified may not have been verified by the study sponsor.
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