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Trial registered on ANZCTR
Registration number
ACTRN12612000563864
Ethics application status
Approved
Date submitted
24/04/2012
Date registered
25/05/2012
Date last updated
7/06/2018
Type of registration
Prospectively registered
Titles & IDs
Public title
A Pilot Study of Topical Honey for the Treatment of
Nappy Rash
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Scientific title
In children less than 5 yrs old with nappy rash is topical medical-grade honey acceptable and does it appear to reduce the severity of nappy rash?
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Secondary ID [1]
280392
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None
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Universal Trial Number (UTN)
U1111-1130-2145
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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:
Nappy Rash
286372
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Condition category
Condition code
Skin
286614
286614
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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
Topical medical grade honey applied to nappy rash in a thin film sufficient to cover the affected area, at each nappy change for 2 weeks.
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Intervention code [1]
284875
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Treatment: Other
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Comparator / control treatment
None
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
287026
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Nappy rash severity assessed by a 5 point nappy rash severity score.
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Assessment method [1]
287026
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Timepoint [1]
287026
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At baseline and at final visit after 2 weeks
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Secondary outcome [1]
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Subjective assessment of nappy rash severity, measured by visual analogue score (VAS)
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Assessment method [1]
297232
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Timepoint [1]
297232
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At baseline and at final visit after 2 weeks
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Secondary outcome [2]
297233
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Objective assessment of global nappy rash severity, measured by VAS
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Assessment method [2]
297233
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Timepoint [2]
297233
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At baseline and at final visit after 2 weeks
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Secondary outcome [3]
297234
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Acceptability of honey therapy, measured by VAS
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Assessment method [3]
297234
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Timepoint [3]
297234
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At final visit after 2 weeks
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Eligibility
Key inclusion criteria
Aged <5 at the time of enrolment
Doctors diagnosis of nappy rash
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Minimum age
No limit
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Maximum age
5
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
Requirement for topical or systemic corticosteroids, as judged by treating doctor
Requirement for antibiotic therapy, as judged by treating doctor
Known or suspected allergy to honey or dressings
Any other condition which, at the investigators discretion, it is believed may present a safety risk or impact the feasibility of the study or the study results
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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
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
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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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Date of first participant enrolment
Anticipated
1/06/2012
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Actual
6/07/2012
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Date of last participant enrolment
Anticipated
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Actual
6/12/2012
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Date of last data collection
Anticipated
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Actual
21/12/2012
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Sample size
Target
10
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Accrual to date
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Final
10
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Recruitment outside Australia
Country [1]
4280
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New Zealand
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State/province [1]
4280
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Bay of Plenty
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Funding & Sponsors
Funding source category [1]
285159
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Commercial sector/Industry
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Name [1]
285159
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Honeylab Ltd
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Address [1]
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Honeylab Ltd
305 Karaka Bay Road
Wellington 6022
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Country [1]
285159
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New Zealand
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Primary sponsor type
Charities/Societies/Foundations
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Name
Medical Research Institute of New Zealand
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Address
Medical Research Institute of New Zealand
Private Bag 7902
Wellington 6242
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Country
New Zealand
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Secondary sponsor category [1]
284022
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None
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Name [1]
284022
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Address [1]
284022
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Country [1]
284022
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
300611
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Multi-region ethics committee
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Ethics committee address [1]
300611
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Ethics committee country [1]
300611
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New Zealand
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Date submitted for ethics approval [1]
300611
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11/04/2012
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Approval date [1]
300611
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30/04/2012
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Ethics approval number [1]
300611
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MEC/12/03/023
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Summary
Brief summary
There are reasons to believe that medical grade-honey applied directly to skin may be an effective treatment for nappy rash. In this study parents/guardians of 10 children with nappy rash will apply medical grade honey to the napkin area at each nappy change. After two weeks the nappy rash will be assessed to look at changes in severity. Participants will also be asked about their experience of using honey. This trial will provide useful information on the practicalities of topical honey as a treatment for nappy rash. It will also give an initial signal as to whether honey may be effective.
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Trial website
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Trial related presentations / publications
Topical kanuka honey for the treatment of nappy rash James Fingleton Christopher Tofield Colin Helm Andrew Corin Mark Weatherall Richard Beasley First published: 06 January 2014 https://doi.org/10.1111/fct.12078
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Public notes
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Contacts
Principal investigator
Name
34111
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Dr James Fingleton
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Address
34111
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Medical Research Institute of New Zealand Private Bag 7902 Wellington 6242
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Country
34111
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New Zealand
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Phone
34111
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+6448051047
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Fax
34111
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Email
34111
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[email protected]
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Contact person for public queries
Name
17358
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James Fingleton
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Address
17358
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Medical Research Institute of New Zealand
Private Bag 7902
Wellington 6242
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Country
17358
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New Zealand
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Phone
17358
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+6448050147
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Fax
17358
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Email
17358
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[email protected]
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Contact person for scientific queries
Name
8286
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James Fingleton
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Address
8286
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Medical Research Institute of New Zealand
Private Bag 7902
Wellington 6242
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Country
8286
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New Zealand
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Phone
8286
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+6448050147
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Fax
8286
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Email
8286
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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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