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A single-center, non-randomized, prospective observational, pilot study designed to determine what is the optimal number of pleural biopsies to take during pleuroscopy.
Full description
After enrollment, participants will undergo pleural biopsies via pleuroscopy. Specimens will be divided into three aliquots (1-3, 4-6, 7-10), which will be sent to pathology. A designated pathologist will evaluate the specimens in each aliquot to determine the number of biopsies required to reach a diagnosis and to obtain sufficient material for biomarker testing (when needed), and determine whether analysis of further aliquots is needed.
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Inclusion criteria
Exclusion criteria
- Inability to provide informed consent
104 participants in 1 patient group
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Central trial contact
Jeeyune Bahk, MBBS BSc
Data sourced from clinicaltrials.gov
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