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Trial registered on ANZCTR
Registration number
ACTRN12609000451202
Ethics application status
Approved
Date submitted
3/06/2009
Date registered
12/06/2009
Date last updated
21/01/2014
Type of registration
Prospectively registered
Titles & IDs
Public title
Burns And Silver In Children: A comparison of the silver based dressings Aquacell and Acticoat for paediatric burns.
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Scientific title
A randomised controlled study of the effect of silver based burns dressings Aquacell and Acticoat on percentage epithelialisation in a paediatric emergency department.
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Secondary ID [1]
283953
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Nil known
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Universal Trial Number (UTN)
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Trial acronym
BASIC
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Burn wounds
236912
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Condition category
Condition code
Injuries and Accidents
237268
237268
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0
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Burns
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Aquacel Ag will be applied to the wound bed with a 3cm overlap to allow for the dressing to shrink. Telfa (an absorbent cotton fabric bonded on both sides with perforated non-adherent film) will be placed over the Aquacel Ag and then Hypafix will be used to hold the dressing in place.
These patients will not be instructed to moisten the dressing at home.
Patients will be reviewed in 3 days after the initial dressing placement. The Hypafix will be removed, and areas of non-adherence will be trimmed and replaced if still considered to be partial thickness and appropriate for outpatient management. Hypafix will then be re-applied.
Patients will be reviewed at day 10 with dressing removal and photography to allow percentage epithelialisation to be assessed
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Intervention code [1]
236701
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Treatment: Other
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Comparator / control treatment
Acticoat3 dressing is applied to the wound bed (blue side down) with a minimum of overlap. The dressing will be moistened with warm water (not saline), and overlapping Hypafix will be used to hold the dressing in place. These patients will be instructed to moisten the dressing three times daily at home with tap water via a spray bottle or shower head.
Patients will be reviewed in 3 days after the initial dressing placement and the Hypafix and Acticoat3 dressings will be removed. These wounds will be visualised, and the wound will be lightly cleaned with saline and re-dressed with Acticoat7 and Hypafix.
Patients will be reviewed at day 10 with dressing removal and photography to allow percentage epithelialisation to be assessed
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Control group
Active
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Outcomes
Primary outcome [1]
238082
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Percentage epithelialisation
This will be assessed using comparison of photo at Day 0 and photo 10 days after initial dressing application by a burns surgeon
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Assessment method [1]
238082
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Timepoint [1]
238082
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10 days following initial application of dressing
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Secondary outcome [1]
242277
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Number of dressing changes
Assessed using chart review
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Assessment method [1]
242277
0
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Timepoint [1]
242277
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10 days following initial application of dressing
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Eligibility
Key inclusion criteria
Partial Thickness Burn (blistering and with normal or increased capillary refill)
Present to Starship Emergency Department within 24 hours of the burn injury
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Minimum age
No limit
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Maximum age
14
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
Superficial epidermal burn (no blistering)
Full-thickness burns and Deep Partial-thickness burns
Partial-thickness burns > 10% Body surface area
Burns to the perineum, genitalia, face, hands or feet (Aquacel Ag contraindicated)
Burns over major joints
Circumferential Burns
Chemical or Electrical burns
Allergy to silver
Patients referred for evaluation of Non-Accidental-Injury
Patients expecting to reside outside Auckland during the 10 day follow-up period.
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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)
Enrollment will occur in the Emergency Department (ED). Once consent has been obtained, sequentially numbered opaque envelopes will be selected that contain treatment allocation information
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Study numbers will be assigned sequentially, and randomization will be achieved by generating numerical codes in random permuted blocks
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people assessing the outcomes
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Intervention assignment
Parallel
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Other design features
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Phase
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
Completed
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Date of first participant enrolment
Anticipated
1/08/2009
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Actual
31/10/2009
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Date of last participant enrolment
Anticipated
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Actual
31/10/2013
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
72
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
1825
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New Zealand
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State/province [1]
1825
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Auckland
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Funding & Sponsors
Funding source category [1]
237091
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Self funded/Unfunded
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Name [1]
237091
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Michael Shepherd
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Address [1]
237091
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Children's Emergency Department
Starship Children's Hospital
Auckland District Health Board
Private Bag 92024
Auckland 1142, New Zealand
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Country [1]
237091
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New Zealand
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Primary sponsor type
Individual
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Name
Michael Shepherd
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Address
Children's Emergency Department
Starship Children's Hospital
Auckland District Health Board
Private Bag 92024
Auckland 1142, New Zealand
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Country
New Zealand
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Secondary sponsor category [1]
4597
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None
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Name [1]
4597
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Address [1]
4597
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Country [1]
4597
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
239192
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Northern X or Y Regional Ethics Committee
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Ethics committee address [1]
239192
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Ethics committee country [1]
239192
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New Zealand
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Date submitted for ethics approval [1]
239192
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15/06/2009
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Approval date [1]
239192
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28/07/2009
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Ethics approval number [1]
239192
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NTX/09/07/061
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Summary
Brief summary
This study aims to determine whether Aquacell is a superior silver based dressing compared to Acticoat for paediatric burns managed as an outpatient .
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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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Dr Michael Shepherd
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Address
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Children's Emergency Department Starship Children's Hospital Auckland District Health Board Private Bag 92024 Auckland 1142, New Zealand
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Country
29690
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New Zealand
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Phone
29690
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+64 9 3074902
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Fax
29690
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Email
29690
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[email protected]
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Contact person for public queries
Name
12937
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Michael Shepherd
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Address
12937
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Children's Emergency Department
Starship Children's Hospital
Auckland District Health Board
Private Bag 92024
Auckland 1142, New Zealand
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Country
12937
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New Zealand
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Phone
12937
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+64 9 3074902
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Fax
12937
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Email
12937
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[email protected]
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Contact person for scientific queries
Name
3865
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Michael Shepherd
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Address
3865
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Children's Emergency Department
Starship Children's Hospital
Auckland District Health Board
Private Bag 92024
Auckland 1142, New Zealand
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Country
3865
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New Zealand
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Phone
3865
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+64 9 3074902
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Fax
3865
0
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Email
3865
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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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