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Portable Conebeam CT Guided Bronchoscopy for Peripheral Pulmonary Lesions: A Pilot Study

Portable Conebeam CT Guided Bronchoscopy for Peripheral Pulmonary Lesions: A Pilot Study - PORT-CBCT BRONC

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000059340
Enrollment
10
Registered
2025-10-08
Start date
2025-12-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

peripheral pulmonary lesions

Interventions

During radial endobronchial ultrasound (EBUS) bronchoscopy for peripheral pulmonary lesions, a portable cone-beam CT system (mobile C-arm, Cios Spin
Siemens Healthcare) is used to confirm the position of the lesion and biopsy tool. One scan is performed, lasting approximately 30 seconds. Reconstructed images are reviewed immediately, and bronchosc

Sponsors

Shimane University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Adult patients (20 years old or older) scheduled to undergo bronchoscopy at Shimane University Hospital Patients with a peripheral pulmonary lesion on imaging for which radial endobronchial ultrasound (EBUS) guided biopsy is clinically indicated Patients who have received a full explanation of the study and provided written informed consent

Exclusion criteria

Exclusion criteria: Patients deemed inappropriate for participation due to radiation exposure considerations Patients judged by the attending physician or bronchoscopist to be unsuitable for inclusion in this study Patients found to be ineligible after consent has been obtained

Design outcomes

Primary

MeasureTime frame
Tool-in-lesion confirmation rate by cone-beam CT

Secondary

MeasureTime frame
Diagnostic image quality achievement rate Artifact score Lesion discernibility score Bronchial visualization rate Examination-related time, compliance with breathing instructions Complications (bleeding, pneumothorax, hypoxia, sedation-related events)

Countries

Japan

Contacts

Public ContactTakamasa Hotta

Shimane University Hospital Division of Medical Oncology & Respiratory Medicine

takamasa@med.shimane-u.ac.jp0853-20-2581

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026