Non-Invasive Testing for PIFI
Diagnostic Testgalactomannan assay, fungal PCRs, cell-free next-generation DNA/RNA sequencing, RNAseq
NCT Number: NCT03827694
This study will establish a non-invasive diagnostic approach and evaluate clinical outcomes for children at high-risk for pulmonary invasive fungal infection (PIFI).
Interested in participating?
Request Info120 day–21 year
All sexes
Observational
The Hospital for Sick Children, Toronto, Ontario, Canada
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
galactomannan assay, fungal PCRs, cell-free next-generation DNA/RNA sequencing, RNAseq
Time frame: Baseline
Time frame: Baseline
Time frame: Baseline
Time frame: Baseline
Time frame: Baseline
Time frame: Baseline
Time frame: Baseline
Time frame: Baseline
Time frame: 49 days
Outcome score inclusive of outcomes and adverse events. Comprehensive clinical outcome score from most to least desirable are score of 1 (survival, improvement in pulmonary nodules, no adverse events related to anti-fungal therapy or invasive diagnostic intervention) to score of 7 (death)
Contact information is provided by the study sponsor or research team.
Arkansas Children's Hospital Research Institute
Other
Acronym: DOMINIC
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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