Clinical Trials Directory

Trials / Completed

CompletedNCT05512533

Feasibility of Thin Cp-EBUS Scope BF-UC290F for the Diagnosis of PPLs

Feasibility and Safety of Thin Convex Probe EBUS Scope BF-UC290F for the Diagnosis of Peripheral Pulmonary Lesions

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
31 (actual)
Sponsor
Shanghai Chest Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study is to evaluate the diagnostic value and safety of Thin Convex Probe Endobronchial Ultrasound (TCP-EBUS) Scope for peripheral pulmonary lesions (PPLs)

Detailed description

This study will determine the feasibility of the novel thin convex probe endobronchial ultrasound (TCP-EBUS) Scope for the diagnosis of peripheral pulmonary lesions. The primary end point is to clarify the feasibility of using the thin convex probe EBUS scope to biopsy peripheral pulmonary lesions. The secondary objective is to evaluate operation time, sample adequacy, factors affecting the diagnosis rate, etc. The safety, insertion ability, and operability of the thin convex probe EBUS would also be evaluated.

Conditions

Interventions

TypeNameDescription
DEVICELinear Ultrasound Bronchoscope BF-UC290F (Olympus)A thin Olympus EBUS bronchoscope BF-UC290F will be used for all endobronchial ultrasound examinations, and biopsies will be conducted with EBUS needles - the ViziShot 2 22G (Olympus).

Timeline

Start date
2022-09-02
Primary completion
2023-02-12
Completion
2023-07-12
First posted
2022-08-23
Last updated
2025-06-05

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05512533. Inclusion in this directory is not an endorsement.