U.S., Nov. 29 -- ClinicalTrials.gov registry received information related to the study (NCT07253727) titled 'The LUCENT Study - LUng Lesion Assessment Via BF-UCP190F for Central and Extended Nodal Targeting' on Nov. 14.
Brief Summary: The Olympus BF-UCP190F bronchoscope combines the reach of a thinner bronchoscope with the benefit of real-time ultrasound, enabling direct lesion visualization and sampling deeper into the lung. Following promising first-in-human data, the LUCENT study aims to evaluate the utility feasibility, effectiveness and safety of this device in a multicenter setting, generating real-world evidence to inform broader adoption in global markets.
Study Start Date: Dec. 01
Study Type: OBSERVATIONAL
Condition:
Bronchosc...