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Trial registered on ANZCTR
Registration number
ACTRN12625000480482
Ethics application status
Approved
Date submitted
21/02/2025
Date registered
19/05/2025
Date last updated
19/05/2025
Date data sharing statement initially provided
19/05/2025
Type of registration
Retrospectively registered
Titles & IDs
Public title
Drug allergy diagnostics, immunology, genomics (DALE) - A prospective registry and biorepository
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Scientific title
Drug allergy diagnostics, immunology, genomics (DALE) - A prospective registry and biorepository for patients with drug allergy
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Secondary ID [1]
314035
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None
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Universal Trial Number (UTN)
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Trial acronym
DALE
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Drug allergy
336779
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Condition category
Condition code
Inflammatory and Immune System
333269
333269
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0
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Allergies
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Intervention/exposure
Study type
Observational
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Patient registry
True
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Target follow-up duration
12
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Target follow-up type
Months
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Description of intervention(s) / exposure
Patients with a reported drug allergy that have been reviewed clinically as an inpatient or outpatient at participating centres will be included in the registry through a waiver of consent, both retrospectively and prospectively. Demographic, medical history, allergy history and allergy testing results will be included. Participants may also be invited to participate actively by donating research samples including blood, skin biopsy, blister fluid for immunological analysis at baseline, 3 months and 12 months post-enrolment. These active participants will also be requested to complete the DrHy-Q at baseline and 12 months post-enrolment. Any pre-existing drug allergy data from the medical record will be reviewed and may be collected retrospectively.
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Intervention code [1]
330616
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Not applicable
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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The number of participants with a reported drug allergy included in the registry per year
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Assessment method [1]
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DALE registry records will be reviewed to obtain count data for the number of participants per year
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Timepoint [1]
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Data will be reviewed annually until the closure of the registry
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Secondary outcome [1]
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Nil
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Assessment method [1]
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Not applicable
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Timepoint [1]
445216
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Not applicable
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Eligibility
Key inclusion criteria
Patients with a reported drug allergy
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Minimum age
18
Years
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Maximum age
No limit
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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
Nil
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Study design
Purpose
Screening
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Duration
Longitudinal
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Selection
Defined population
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Timing
Both
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Statistical methods / analysis
The study is observational and exploratory; therefore, no sample size has been calculated.
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
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Actual
13/02/2025
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Date of last participant enrolment
Anticipated
15/02/2035
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Actual
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Date of last data collection
Anticipated
14/02/2036
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Actual
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Sample size
Target
3000
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Accrual to date
1
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Final
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Recruitment in Australia
Recruitment state(s)
NSW,VIC
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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The University of Melbourne
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Address [1]
318542
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Country [1]
318542
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Australia
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Primary sponsor type
University
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Name
The University of Melbourne
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Address
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Country
Australia
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Secondary sponsor category [1]
320938
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Hospital
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Name [1]
320938
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Austin Health
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Address [1]
320938
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Country [1]
320938
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
317142
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Austin Health Human Research Ethics Committee
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Ethics committee address [1]
317142
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https://www.austin.org.au/Office-for-Research/
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Ethics committee country [1]
317142
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Australia
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Date submitted for ethics approval [1]
317142
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16/08/2024
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Approval date [1]
317142
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06/02/2025
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Ethics approval number [1]
317142
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Summary
Brief summary
DALE is a prospective, multi-site registry and biorepository, established to facilitate the collection of clinical data and biospecimens with the aim of furthering drug allergy research. Research questions which may be addressed relate to the epidemiology of drug allergy, our mechanistic understanding of the immune response to drugs in allergic patients, predictors of true or false drug allergy, diagnostic methods to identify causative drugs and quality of care in the management of drug allergy and delabelling.
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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 Jason Trubiano
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Address
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Department of Infectious Diseases and Immunology, Austin Hospital, 145 Studley Road, Heidelberg VIC 3084
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Country
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Australia
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Phone
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+61 3 9496 6676
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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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Fiona James
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Address
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Department of Infectious Diseases and Immunology, Austin Hospital, 145 Studley Road, Heidelberg VIC 3084
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Country
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Australia
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Phone
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+61 3 9496 6676
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
140144
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Jason Trubiano
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Address
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Department of Infectious Diseases and Immunology, Austin Hospital, 145 Studley Road, Heidelberg VIC 3084
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Country
140144
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Australia
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Phone
140144
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+61 3 9496 6676
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Fax
140144
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Email
140144
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[email protected]
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Data sharing statement
Will the study consider sharing individual participant data?
Yes
Will there be any conditions when requesting access to individual participant data?
Persons/groups eligible to request access:
•
Researchers
Conditions for requesting access:
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Yes, conditions apply:
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Requires review on a case-by-case basis by the trial custodian, sponsor or data sharing committee
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Requires a scientifically sound proposal or protocol
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Requires approval by an ethics committee
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Requires a data sharing agreement between data requester and trial custodian or sponsor
What individual participant data might be shared?
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All de-identified individual participant data
What types of analyses could be done with individual participant data?
•
Any type of analysis (i.e. no restrictions on data re-use)
When can requests for individual participant data be made (start and end dates)?
From:
13/02/2025
To:
Not yet decided
Where can requests to access individual participant data be made, or data be obtained directly?
•
Email of trial custodian, sponsor or committee:
[email protected]
Are there extra considerations when requesting access to individual participant data?
No
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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