Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12610000501044
Ethics application status
Approved
Date submitted
27/04/2010
Date registered
17/06/2010
Date last updated
8/01/2020
Date data sharing statement initially provided
8/01/2020
Type of registration
Retrospectively registered

Titles & IDs
Public title
Folate Absorption Study in Healthy Adults
Scientific title
Relative Bioavailability of Microencapsulated Reduced Folate versus Folic Acid in Healthy Adult Volunteers
Secondary ID [1] 251822 0
nil
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Folate status in healthy adults 257246 0
Condition category
Condition code
Diet and Nutrition 257386 257386 0 0
Other diet and nutrition disorders

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
This randomised crossover study will be conducted in sixteen healthy adults. Participants will attend 8 morning clinics approximately 1 week apart. Participants will be assigned to one of 8 treatments each week using a balanced design; 1) placebo (methyl cellulose), 2) 0.4 mg non-microencapsulated folic acid, 3) 0.4 mg non-microencapsulated L-5-methyltetrahydrofolate (L-MTHF) 4) 0.4 mg microencapsulated folic acid with 75% stearate coating, 5) 0.4 mg microencapsulated L-MTHF with 75% stearate coating 6) 0.4 mg microencpaulsated folic acid with 25% stearate coating 7) 0.4 mg microencapsulated folic acid with 75% stearate coating in milk powder, 8) 0.4 mg microencapsulated L-MTHF with 75% stearate coating in milk powder. Treatments 1 through 6 will be given in capsule form and treatments 7 and 8 will be given in milk powder. At each visit, a venous catheter will be inserted and a baseline blood sample drawn. The participants will then be instructed to consume a capsule or milk containing the folate or placebo. Blood samples (5 ml) will be drawn every 1/4 hour for the first two hours and then every 1/2 hour for the next 2 hours and then every hour for an additional four hours. A standardized low folate breakfast and lunch will be offered between baseline and ½ hour blood collections and between the 4 and 5 hour blood collections, respectively.
Intervention code [1] 256366 0
Treatment: Other
Intervention code [2] 256677 0
Prevention
Comparator / control treatment
Placebo containing no folate (see above)
Control group
Placebo

Outcomes
Primary outcome [1] 258303 0
Plasma folate levels over eight hours after ingestion of folate or placebo. Area under the curve of plasma folate.
Timepoint [1] 258303 0
8 treatments one week apart.

At each visit a baseline blood sample will be drawn, the folate or placebo pill taken and blood collected every 1/4 hour for the first two hours and then every 1/2 hour for the next 3 hours and then every hour for an additional four hours.
Secondary outcome [1] 264001 0
None
Timepoint [1] 264001 0
None

Eligibility
Key inclusion criteria
- Males and Females aged 18-65 years
Minimum age
18 Years
Maximum age
65 Years
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
Vitamin supplement users
- People with a chronic disease e.g. heart disease, diabetes
- People with allergies to milk
-Men and women with anemia at baseline. (Haemoglobin (Hb) <120 /L females <140 g/L males)
-People taking drugs know to interefere with folate metabolism (i.e. methotextrate, sulphasalazine, phenytoin, and others)

Study design
Purpose of the study
Prevention
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
There are 8 different treatments. Each participant will be assigned to a random sequence. Allocation is concealed from participant but not investigator
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
A random sequence generated using online randomization tool. Participants were randomized to the sequences.
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



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

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
25/04/2010
Actual
5/05/2010
Date of last participant enrolment
Anticipated
Actual
25/06/2010
Date of last data collection
Anticipated
Actual
25/09/2010
Sample size
Target
16
Accrual to date
Final
16
Recruitment outside Australia
Country [1] 2604 0
New Zealand
State/province [1] 2604 0

Funding & Sponsors
Funding source category [1] 256875 0
Government body
Name [1] 256875 0
Advanced Foods and Materials Network (AFMNet) - Networks of Centres of Excellence (NCE)
Country [1] 256875 0
Canada
Primary sponsor type
University
Name
University of Otago
Address
PO Box 56
Dunedin 9054
Country
New Zealand
Secondary sponsor category [1] 256147 0
University
Name [1] 256147 0
University of British Columbia
Address [1] 256147 0
2205 East Mall, Vancouver, BC, V6T 1Z4
Country [1] 256147 0
Canada
Other collaborator category [1] 1220 0
Commercial sector/Industry
Name [1] 1220 0
Merck Eprova
Address [1] 1220 0
Im Laternenacker 5, 8200 Schaffhausen,
Country [1] 1220 0
Switzerland

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 258882 0
University of Otago
Ethics committee address [1] 258882 0
Ethics committee country [1] 258882 0
Date submitted for ethics approval [1] 258882 0
Approval date [1] 258882 0
10/02/2010
Ethics approval number [1] 258882 0

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

Contacts
Principal investigator
Name 31096 0
Address 31096 0
Country 31096 0
Phone 31096 0
Fax 31096 0
Email 31096 0
Contact person for public queries
Name 14343 0
Sarah Harvey
Address 14343 0
PO Box 56
Dunedin 9054
New Zealand
Country 14343 0
New Zealand
Phone 14343 0
64 3 479 5839
Fax 14343 0
Email 14343 0
[email protected]
Contact person for scientific queries
Name 5271 0
Tim Green
Address 5271 0
Human Nutrition
University of British Columbia, 2205 East Mall, Vancouver, BC, V6T 1Z4
Country 5271 0
Canada
Phone 5271 0
+1 604 822 0421
Fax 5271 0
Email 5271 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No/undecided IPD sharing reason/comment


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.