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UnknownNCT05402176

The SHIELD Whole Lung Lavage Study

Silicosis - Harnessing New Ideas to Conquer the Re-emergence of an Ancient Lung Disease: The SHIELD Whole Lung Lavage Study

Status
Unknown
Phase
Study type
Observational
Enrollment
30 (estimated)
Sponsor
The University of Queensland · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

An observational cohort study that will assess the efficacy of Whole Lung Lavage in workers with silicosis or silica-induced bronchitis.

Detailed description

BACKGROUND: Silicosis is a fatal lung disease caused by inhaling silica particles. Australia is currently facing an epidemic with hundreds of young workers having contracted silicosis from machining engineered stone. AIMS: To determine the effectiveness and safety of Whole Lung Lavage (WLL) in workers with silicosis due to significant engineered stone exposure. DESIGN: Participants (30) with silicosis or silica-induced bronchitis who are scheduled to undergo WLL as part of their normal care will be enrolled. They will undergo the following interventions pre and 3 months post WLL, some of which would have been carried out as part of routine standard care: 1. Complex pulmonary function tests (PFTs) - standard care 2. HRCT scan (if not within 6 months of WLL) - standard care 3. Blood tests 4. Cardiopulmonary exercise testing 5. Forced oscillatory technique 6. XV Lung Ventilation Analysis 7. Questionnaires (K-BILD and LCQ)

Conditions

Interventions

TypeNameDescription
OTHERWhole Lung LavageWhole Lung Lavage (WLL) is performed as standard of care. Outcome following WLL is observed.

Timeline

Start date
2022-06-01
Primary completion
2024-06-01
Completion
2024-12-01
First posted
2022-06-02
Last updated
2022-06-02

Locations

4 sites across 1 country: Australia

Source: ClinicalTrials.gov record NCT05402176. Inclusion in this directory is not an endorsement.