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Trial registered on ANZCTR
Registration number
ACTRN12612000570886
Ethics application status
Approved
Date submitted
28/05/2012
Date registered
28/05/2012
Date last updated
20/07/2018
Type of registration
Prospectively registered
Titles & IDs
Public title
Vitamin D in the management of Childhood Atopic Dermatitis (eczema)
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Scientific title
In children aged 2-16 with moderate to severe atopic dermatitis (eczema), is daily vitamin D3 (1000 IU/day) more effective than placebo in improving the severity of the eczema and quality of life.
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Secondary ID [1]
280561
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nil
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Universal Trial Number (UTN)
U1111-1131-2345
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Trial acronym
ADDVIT
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Atopic Dermatitis
286564
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Condition category
Condition code
Inflammatory and Immune System
286833
286833
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0
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Allergies
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Skin
286837
286837
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0
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Dermatological conditions
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Eligible children recruited and enrolled will be randomised to receive either liquid drops of Vitamin D 3 (Cholecalciferol)(1000 IU/day) or placebo for a period of 3 months. All children enrolled will be allowed to continue their normal skin care regime, with use of moisturisers and topical steroids throughout the study period.
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Intervention code [1]
284946
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Treatment: Drugs
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Comparator / control treatment
placebo- liquid vehicle with no Vitamin D3
All children enrolled will be allowed to continue their normal skin care regime, with use of moisturisers and topical steroids throughout the study period.
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Control group
Placebo
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Outcomes
Primary outcome [1]
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Eczema severity score (SCORAD)
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Assessment method [1]
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Timepoint [1]
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t=0, t=1.5 and t=3 (0, 6 weeks and 3 months)
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Secondary outcome [1]
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Use of topical steroid (frequency, potency)
By specially designed parent daily recording diary.
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Assessment method [1]
297595
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Timepoint [1]
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t=0, t=1.5 and t=3 (0, 6 weeks and 3 months)
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Secondary outcome [2]
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Quality of life (QoL),
By previously published quality of life in eczema in childhood and eczema in infants questionaires. Parents fill in the infant questionaire. the child questionaire is designed for children aged >4 to complete.
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Assessment method [2]
297600
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Timepoint [2]
297600
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t=0, t=1.5 and t=3 (0, 6 weeks and 3 months)
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Secondary outcome [3]
297601
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Treg phenotype
T cells are phenotyped by colour flow cytometry and analuyed by FACS.
T reg cell function is detremined by in vitro cellular supression culture assay
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Assessment method [3]
297601
0
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Timepoint [3]
297601
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t=0, t=3 months
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Secondary outcome [4]
297602
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Vitamin D status
By laboratory measurement of Vitamin D level in serum
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Assessment method [4]
297602
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Timepoint [4]
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t=0, t=3 months
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Eligibility
Key inclusion criteria
Inclusion criteria-
Atopic dermatitis consistent with diagnostic criteria of Hanifin and Rajka.
Ages- 2 years- 16 years
Moderate-severe eczema at study entry defined as an objective SCORAD of > 15 (0-83)
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Minimum age
2
Years
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Maximum age
16
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
Exclusion Criteria
Ages <2 years or >16 years
Past or current history of oral immunosuppression therapy (Cyclosporin, Azathioprine, Methotrexate)
Oral corticosteroids < 6 months prior to study
IVIg therapy< 2 years prior to study
Hypercalcaemia, Hypertension, Anticonvulsant therapy
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Study design
Purpose of the study
Treatment
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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)
Children will randomly allocated in a 1:1 ratio to "Vit D" and "Placebo" treatments. Treatment allocation will stratified by gender.
Numbered containers with central randomisation by computer with code held by one designated person not involved with any other aspects of the trial.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Allocation used permuted blocks to maintain treatment balance over time, and blocks will be a random mixture of sizes to assist allocation concealment
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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
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Phase
Phase 2 / Phase 3
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
1/07/2012
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Actual
11/03/2013
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Date of last participant enrolment
Anticipated
31/12/2018
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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
150
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Accrual to date
36
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Final
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Recruitment in Australia
Recruitment state(s)
NSW
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Recruitment hospital [1]
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The Children's Hospital at Westmead - Westmead
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Recruitment postcode(s) [1]
23497
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2145 - Westmead
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Funding & Sponsors
Funding source category [1]
285326
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Hospital
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Name [1]
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Department of Allergy and Immunology, Childrens Hospital Westmead
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Address [1]
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Childrens Hospital Westemad
Hawkesbury rd
Westmead
NSW 2145
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Country [1]
285326
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Australia
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Primary sponsor type
Individual
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Name
Prof Dianne Campbell
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Address
Childrens Hospital Westemad
Hawkesbury rd
Westmead
NSW 2145
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Country
Australia
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Secondary sponsor category [1]
284180
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Individual
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Name [1]
284180
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Professor Ralph Nanan
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Address [1]
284180
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Nepean clinical School
Nepean Hospital
Derby St, Kingswood, NSW 2747
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Country [1]
284180
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
287342
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Sydney Childrens Hopsitals Network HREC
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Ethics committee address [1]
287342
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Hawkesbury Rd CHW Westmead NSW 2145
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Ethics committee country [1]
287342
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Australia
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Date submitted for ethics approval [1]
287342
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02/03/2012
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Approval date [1]
287342
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14/11/2012
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Ethics approval number [1]
287342
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12/SCHN/24
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Summary
Brief summary
The project aims to show that oral vitamin D supplementation will improve the severity of childhood atopic dermatitis (eczema). We will compare the severity of disease in children with moderate-severe atopic dermatitis after 3 months of daily Vitamin D therapy or placebo, using randomised double blind placebo controlled methodology. We propose that the severity of moderate and moderate-severe atopic dermatitis will be significantly decreased by oral Vitamin D therapy. We aim to show that in these children, following 3 months of daily vitamin D3 at 1000IU, there will be a significant decrease in their disease severity and decreased use of topical corticosteroids. We aim to demonstrate a significant improvement in the quality of life for these children, as measured by a validated quality of life questionnaire.
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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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Prof Dianne E Campbell
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Address
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Department of Allergy and Immunology
Locked Bag 4001
Children's Hospital Westmead, Sydney
NSW 2145
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Country
34229
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Australia
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Phone
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+61298453420
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Dianne Campbell
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Address
17476
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Department of Allergy and Immunology
CHW, Hawkesbury Rd
Westmead
NSW
2145
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Country
17476
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Australia
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Phone
17476
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+61298453420
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Fax
17476
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+61298453389
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Email
17476
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[email protected]
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Contact person for scientific queries
Name
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Dianne Campbell
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Address
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Department of Allergy and Immunology
CHW,Hawkesbury Rd
Westmead
NSW
2145
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Country
8404
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Australia
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Phone
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+61298453420
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Fax
8404
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+61298453389
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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
No additional documents have been identified.
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