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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00801957
Registration number
NCT00801957
Ethics application status
Date submitted
3/12/2008
Date registered
4/12/2008
Date last updated
18/09/2014
Titles & IDs
Public title
Equivalence of the Response to Vaccination of Tacrolimus Ointment to a Steroid Ointment Regimen in Children With Atopic Dermatitis
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Scientific title
A Double Blind, Multicentre, Randomised, Parallel Group Study to Demonstrate the Equivalence of the Response to Vaccination of a Tacrolimus Ointment Regimen to a Steroid Ointment Regimen in Children With Moderate to Severe Atopic Dermatitis
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Secondary ID [1]
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FG-506-06-27
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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:
Atopic Dermatitis
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Condition category
Condition code
Skin
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Dermatological conditions
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Skin
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Other skin conditions
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Inflammatory and Immune System
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0
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Other inflammatory or immune system disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Drugs - tacrolimus ointment 0.03%
Treatment: Drugs - hydrocortisone acetate ointment 1%
Treatment: Drugs - hydrocortisone butyrate ointment 0.1%
Treatment: Other - Meningitec
Treatment: Other - AC VAX
Experimental: 1 - tacrolimus ointment 0.03%
Active comparator: 2 - hydrocortisone acetate 1% and butyrate 0.1%
Other: 3 - Control group vaccination and challenge dose only
Treatment: Drugs: tacrolimus ointment 0.03%
topical application
Treatment: Drugs: hydrocortisone acetate ointment 1%
topical application
Treatment: Drugs: hydrocortisone butyrate ointment 0.1%
topical application
Treatment: Other: Meningitec
im injection
Treatment: Other: AC VAX
im injection
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Intervention code [1]
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Treatment: Drugs
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Intervention code [2]
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Treatment: Other
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Percentage of patients with serum bactericidal antibody titer of = 8
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Assessment method [1]
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Timepoint [1]
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5 weeks
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Secondary outcome [1]
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Assessment of other immunological parameters
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Assessment method [1]
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Timepoint [1]
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7 months
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Eligibility
Key inclusion criteria
* Patients with moderate to severe atopic dermatitis and in need for treatment
* Patients require vaccination to prevent invasive disease caused by Neisseria meningitidis serogroup C
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Minimum age
2
Years
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Maximum age
11
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
* Patients have known hypersensitivity to macrolides, tacrolimus and any component of the vaccine
* Patients have an acute severe febrile illness, genetic epidermal barrier defect such as Netherton's syndrome or generalized erythroderma, a skin infection on the affected and to be treated area
* Patients have already received a meningo polysaccharide or conjugated vaccine against meningitis
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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)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 2
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
1/03/2003
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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
1/11/2004
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Sample size
Target
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Accrual to date
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Final
260
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Recruitment in Australia
Recruitment state(s)
NSW,QLD,SA,VIC,WA
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Recruitment hospital [1]
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- Kogarah
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Recruitment hospital [2]
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- St. Leonards
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Recruitment hospital [3]
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- Benowa
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Recruitment hospital [4]
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- Carina Heights
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Recruitment hospital [5]
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- Herston
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Recruitment hospital [6]
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- North Adelaide
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Recruitment hospital [7]
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- Carlton
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Recruitment hospital [8]
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- Parkville
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Recruitment hospital [9]
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- Fremantle
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Recruitment postcode(s) [1]
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2217 - Kogarah
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Recruitment postcode(s) [2]
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2065 - St. Leonards
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Recruitment postcode(s) [3]
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4217 - Benowa
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Recruitment postcode(s) [4]
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4152 - Carina Heights
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Recruitment postcode(s) [5]
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4029 - Herston
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Recruitment postcode(s) [6]
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5006 - North Adelaide
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Recruitment postcode(s) [7]
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3053 - Carlton
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Recruitment postcode(s) [8]
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3052 - Parkville
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Recruitment postcode(s) [9]
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6160 - Fremantle
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Recruitment outside Australia
Country [1]
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Belgium
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State/province [1]
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Leuven
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Germany
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Bretten
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Germany
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Ettenheim
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Germany
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Gersfeld
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Germany
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Kehl
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Germany
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Tettnang
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Hungary
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Budapest
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Hungary
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Debrecen
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Hungary
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Pecs
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Hungary
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Szeged
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Iceland
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Kopavogur
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Malta
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St. Julians
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Poland
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Karpacz
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Poland
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Krakow
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Lodz
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Poland
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Opole
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Poland
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Poznan
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Poland
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Rabka-Zdroj
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Poland
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Warszawa
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Wroclaw
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Poland
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Zabrze
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Poland
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Zgierz
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Portugal
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State/province [23]
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Lisboa
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Portugal
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State/province [24]
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Porto
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Astellas Pharma Inc
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
Seven-month study in pediatric patients (2-11 years) with moderate to severe AD who were considered to benefit from vaccination to prevent invasive disease caused by Neisseria meningitides serogroup C.
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Trial website
https://clinicaltrials.gov/study/NCT00801957
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Trial related presentations / publications
Hofman T, Cranswick N, Kuna P, Boznanski A, Latos T, Gold M, Murrell DF, Gebauer K, Behre U, Machura E, Olafsson J, Szalai Z; International Tacrolimus Ointment Study Group. Tacrolimus ointment does not affect the immediate response to vaccination, the generation of immune memory, or humoral and cell-mediated immunity in children. Arch Dis Child. 2006 Nov;91(11):905-10. doi: 10.1136/adc.2006.094276. Epub 2006 Jun 23. Erratum In: Arch Dis Child. 2007 Jan;92(1):93.
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Public notes
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Contacts
Principal investigator
Name
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Central Contact
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Address
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Astellas Pharma Europe B.V.
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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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Address
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Contact person for scientific queries
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
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT00801957
Download to PDF