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Please note the ANZCTR will be unattended on Monday the 27th of January due to the national public holiday.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this information for consumers
Trial registered on ANZCTR


Registration number
ACTRN12625000083493
Ethics application status
Approved
Date submitted
21/02/2025
Date registered
21/02/2025
Date last updated
21/02/2025
Date data sharing statement initially provided
21/02/2025
Type of registration
Prospectively registered

Titles & IDs
Public title
Test ANZCTR-11 Removed Old IPD Display
Scientific title
Test ANZCTR-11 Removed Old IPD Display
Secondary ID [1] 313823 0
12314145
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
test 336452 0
Condition category
Condition code
Blood 332973 332973 0 0
Anaemia

Intervention/exposure
Study type
Observational
Patient registry
False
Target follow-up duration
Target follow-up type
Description of intervention(s) / exposure
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Intervention code [1] 330405 0
Not applicable
Comparator / control treatment
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Control group
Active

Outcomes
Primary outcome [1] 340512 0
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Timepoint [1] 340512 0
test
Secondary outcome [1] 444284 0
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Timepoint [1] 444284 0
test

Eligibility
Key inclusion criteria
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Minimum age
20 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
test

Study design
Purpose
Duration
Selection
Timing
Statistical methods / analysis

Recruitment
Recruitment status
Not yet recruiting
Date of first participant enrolment
Anticipated
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
NSW
Recruitment hospital [1] 27525 0
The Hills Clinic - Kellyville
Recruitment postcode(s) [1] 43637 0
2155 - Kellyville

Funding & Sponsors
Funding source category [1] 318290 0
Government body
Name [1] 318290 0
test
Country [1] 318290 0
Australia
Primary sponsor type
Hospital
Name
Test
Address
Country
Australia
Secondary sponsor category [1] 320678 0
None
Name [1] 320678 0
Address [1] 320678 0
Country [1] 320678 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 316933 0
Aboriginal Health & Medical Research Council Ethics Committee
Ethics committee address [1] 316933 0
Ethics committee country [1] 316933 0
Australia
Date submitted for ethics approval [1] 316933 0
21/02/2025
Approval date [1] 316933 0
21/02/2025
Ethics approval number [1] 316933 0

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 139486 0
Mr Nathan Leung
Address 139486 0
test
Country 139486 0
Australia
Phone 139486 0
+61 412345678
Fax 139486 0
Email 139486 0
Contact person for public queries
Name 139487 0
Nathan Leung
Address 139487 0
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Country 139487 0
Australia
Phone 139487 0
+61 412345678
Fax 139487 0
Email 139487 0
Contact person for scientific queries
Name 139488 0
Nathan Leung
Address 139488 0
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Country 139488 0
Australia
Phone 139488 0
+61 412345678
Fax 139488 0
Email 139488 0

Data sharing statement
Will the study consider sharing individual participant data?
Yes
Will there be any conditions when requesting access to individual participant data?
Who can request access to individual participant data?
Researchers
Other
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Are there any conditions for requesting access to individual participant data?
No requirements
What individual participant data might be shared?
De-identified individual participant data Published results Primary outcome(s) Safety data
What types of analyses could be done with individual participant data?
Systematic reviews and meta-analyses
Studies exploring new research questions
Studies testing whether findings can be repeated or confirmed
When can requests for individual participant data be made (start and end dates)?
From:
Other
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To:
A finite period of 1 years
Where can requests to access individual participant data be made, or data be obtained directly?
Journal publication or its supplementary materials
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Are there extra considerations when requesting access to individual participant data?
No
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No/undecided IPD sharing reason/comment


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.