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Trial registered on ANZCTR
Registration number
ACTRN12605000258651
Ethics application status
Approved
Date submitted
25/08/2005
Date registered
1/09/2005
Date last updated
21/09/2011
Type of registration
Retrospectively registered
Titles & IDs
Public title
The antioxidant and immunomodulatory effects of Ambrotose AO in healthy smokers and non-smokers
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Scientific title
The antioxidant and immunomodulatory effects of Ambrotose AO in healthy smokers and non-smokers
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Antioxidant activity and immune function
345
0
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Condition category
Condition code
Inflammatory and Immune System
398
398
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0
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Normal development and function of the immune system
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Ambrotose AO
Week 1 - Baseline 1;
Week 2 - Baseline 2;
Week 3 - 2 capsules daily;
Week 4 - 4 capsules daily
Week 5 - 8 capsules daily
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Intervention code [1]
263
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Treatment: Other
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Comparator / control treatment
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Ex vivo changes in serum oxygen radical capacity.
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Assessment method [1]
459
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Timepoint [1]
459
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Measured week 3, week 4, week 5, week 6.
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Secondary outcome [1]
997
0
In vivo changes in lymphocyte subsets
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Assessment method [1]
997
0
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Timepoint [1]
997
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Measured weekly
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Secondary outcome [2]
998
0
Urinary iPF2
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Assessment method [2]
998
0
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Timepoint [2]
998
0
Measured weekly
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Secondary outcome [3]
999
0
Phagocytosis of granulocytes and monocytes
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Assessment method [3]
999
0
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Timepoint [3]
999
0
Measured weekly
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Secondary outcome [4]
1000
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COX 2 activity
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Assessment method [4]
1000
0
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Timepoint [4]
1000
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Measured weekly
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Eligibility
Key inclusion criteria
1. Individuals willing to cease all medications over the course of the study, excluding medications for acute conditions such as pain or dyspepsia.
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Minimum age
18
Years
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Maximum age
50
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
1. Individuals taking antioxidant medications and/or supplements2. Individuals with poor venous access3. Individuals with auto-immune disorders4. Individuals with diabetes5. Individuals taking immune suppressant drugs6. Individuals taking cytokine or interferon therapy7. Individuals taking Echinacea or other immune stimulating herbs8. Individuals with clinically abnormal liver function tests at baseline9. Individuals unwilling to have blood taken 9 times during the study10. Individuals unwilling to comply with the study protocols11. Individuals with any other condition which in the opinion of the researchers could compromise the study.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
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Phase
Phase 3
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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
15/11/2004
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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
20
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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]
450
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Commercial sector/Industry
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Name [1]
450
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Mannatech
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Address [1]
450
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Country [1]
450
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Primary sponsor type
Commercial sector/Industry
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Name
Mannatech
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Address
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Country
United States of America
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Secondary sponsor category [1]
367
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None
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Name [1]
367
0
none
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Address [1]
367
0
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Country [1]
367
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
1424
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Southern Cross University Human Research Ethics Committee
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Ethics committee address [1]
1424
0
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Ethics committee country [1]
1424
0
Australia
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Date submitted for ethics approval [1]
1424
0
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Approval date [1]
1424
0
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Ethics approval number [1]
1424
0
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Summary
Brief summary
The project was an open label, forced titration dose response study conducted over 5 weeks in 10 healthy smokers and 10 healthy non-smokers. Twenty-two subjects were enrolled in the study and were similarly treated with the study medication. Data was collected at baseline and then each week for a further 5 weeks.
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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
35299
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Address
35299
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Country
35299
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Phone
35299
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Fax
35299
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Email
35299
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Contact person for public queries
Name
9452
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Professor Stephen Myers
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Address
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Australian Centre for Complementary Medicine Education and Research (ACCMER)
PO Box 157
Lismore NSW 2480
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Country
9452
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Australia
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Phone
9452
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+61 2 66203403
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Fax
9452
0
+61 2 66203307
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Email
9452
0
[email protected]
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Contact person for scientific queries
Name
380
0
Joan O'Connor
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Address
380
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Australian Centre for Complementary Medicine Education and Research (ACCMER)
PO Box 157
Lismore NSW 2480
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Country
380
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Australia
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Phone
380
0
+61 2 66203649
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Fax
380
0
+61 2 66203307
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Email
380
0
[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
A forced titration study of the antioxidant and immunomodulatory effects of Ambrotose AO supplement
2010
https://doi.org/10.1186/1472-6882-10-16
N.B. These documents automatically identified may not have been verified by the study sponsor.
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