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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT05546944
Registration number
NCT05546944
Ethics application status
Date submitted
15/09/2022
Date registered
21/09/2022
Date last updated
21/09/2022
Titles & IDs
Public title
The SHIELD Study-silicosis
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Scientific title
Silicosis-harnessing New Ideas to Conquer the Re-emergence of an Ancient Lung Disease
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Secondary ID [1]
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SHIELD
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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:
Silicosis
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Condition category
Condition code
Respiratory
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Other respiratory disorders / diseases
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Intervention/exposure
Study type
Observational [Patient Registry]
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
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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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the SHIELD study primary outcome is to build up knowledge gap to accurately diagnose silicosis, as well as predict disease progress, assess response to treatment, hasten therapeutic discovery in 12 months.
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Assessment method [1]
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1. Establish the SHIELD cohort and associated lung fluid, tissue and blood biobank from well phenotyped RCS-exposed workers identified via the screening programs.
2. Utilise advanced microscopy, 'omic platforms and single cell RNA sequencing (scRNAseq) alongside conventional laboratory techniques, to identify and validate candidate lung and blood biomarkers associated with disease and disease progression at 12 months.
3. To evaluate associations between baseline characteristics, biomarkers and progression of disease in the full cohort.
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Timepoint [1]
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12 months
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Eligibility
Key inclusion criteria
* All workers with a history of significant engineered stone exposure will be potentially eligible.
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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
-
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Study design
Purpose
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Duration
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Selection
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Timing
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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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
16/08/2022
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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
1/12/2024
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Actual
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Sample size
Target
120
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
QLD
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Recruitment hospital [1]
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The Prince Charles Hospital - Brisbane
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Recruitment postcode(s) [1]
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- Brisbane
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Funding & Sponsors
Primary sponsor type
Other
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Name
The University of Queensland
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Address
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Country
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Other collaborator category [1]
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Government body
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Name [1]
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The Prince Charles Hospital
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Address [1]
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Country [1]
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Other collaborator category [2]
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Other
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Name [2]
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Royal Prince Alfred Hospital, Sydney, Australia
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Address [2]
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Country [2]
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Other collaborator category [3]
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Other
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Name [3]
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The Alfred
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Address [3]
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Country [3]
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Other collaborator category [4]
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Other
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Name [4]
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Austin Hospital, Melbourne Australia
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Address [4]
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Country [4]
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Ethics approval
Ethics application status
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Summary
Brief summary
An observational cohort study to derive biomarkers which are able to more accurately diagnose silicosis, as well as predict disease progression, assess response to treatment, and hasten therapeutic discovery.
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Trial website
https://clinicaltrials.gov/study/NCT05546944
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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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Daniel Chambers
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Address
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The Prince Charles Hospital
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Country
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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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Daniel Chambers
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Address
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Country
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Phone
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(07) 3646 7498
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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
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/NCT05546944
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