Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT07253727

The LUCENT Study - LUng Lesion Assessment Via BF-UCP190F for Central and Extended Nodal Targeting

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
200 (estimated)
Sponsor
Olympus Europe SE & Co. KG · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
OTHERNo Interventionsno intervention, only observational

Timeline

Start date
2025-12-01
Primary completion
2027-01-31
Completion
2028-08-31
First posted
2025-11-28
Last updated
2025-11-28

Source: ClinicalTrials.gov record NCT07253727. Inclusion in this directory is not an endorsement.