Peripheral Pulmonary Lesions (PPLs)

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Review clinical trials related to Peripheral Pulmonary Lesions (PPLs). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

CLE vs. ROSE for Ex Vivo Lung Biopsy Assessment

The goal of this observational study is to evaluate the diagnostic efficacy of Confocal Laser Endomicroscopy (CLE) compared to Rapid On-Site Evaluation (ROSE) for ex vivo lung biopsy specimens obtained via bronchoscopy. The main questions it aims to answer are: 1. Does CLE provide diagnostic accuracy comparable to ROSE for the real-time assessment of peripheral pulmonary lesions? 2. What is the level of consistency between CLE-detected malignant architectural patterns and ROSE-identified atypical cells? Participants with peripheral pulmonary lesions (5-50 mm) undergoing navigational bronchoscopy will have their first retrieved biopsy specimen sequentially analyzed. The specimen will undergo CLE scanning first, followed immediately by ROSE cytology, before being fixed for final histopathological examination (the gold standard). CLE and ROSE interpreters will be blinded to the final pathological results and to each other's findings. Diagnostic performance, inter-modality agreement (using Kappa statistics), and procedure times will be analyzed to determine if CLE can serve as a non-consumptive alternative to ROSE.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Guangzhou Medical UniversityUpdated: Jul 24, 2026Locations: 1
Eligibility criteria

(1)Imaging Findings: Presence of a peripheral pulmonary lesion (PPL) measuring 5...

(1)Contraindications to Bronchoscopy: Patients with severe cardiopulmonary insuf...

Status: Not yet recruiting

Advanced Robotic Techniques and Rapid Onsite Evaluation for Minimally Invasive Diagnosis and Next-Generation Sequencing.

ARTEMIS is a multicenter randomized controlled trial. The goal is to understand whether rapid onsite evaluation during robotic assisted bronchoscopy improves the diagnostic performance of the procedure or not.

Participants needed: 400
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Vanderbilt University Medical CenterUpdated: Jul 6, 2026Locations: 8
Eligibility criteria

≥ 18 years of age at time of bronchoscopy [+1]

Declines to participate or inability to provide informed consent. [+4]

Status: Not yet recruiting

Shape-sensing Versus Electromagnetic Robotic Bronchoscopy for Evaluation of PulmoNary LEsions

This is an investigator-initiated, multicenter, non inferiority, cluster randomized controlled trial. The primary objective is to compare the diagnostic yield of the electromagnetic robotic assisted bronchoscopy with digital tomosynthesis (Galaxy system by Noah Medical) to the shape sensing robotic assisted bronchoscopy with integrated cone beam CT (Ion™ Endoluminal System by Intuitive) in patients undergoing bronchoscopy for peripheral pulmonary lesion (PPL) evaluation.

Participants needed: 346
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: The Cleveland ClinicUpdated: May 28, 2026Locations: 2
Eligibility criteria

≥ 18 years of age at time of bronchoscopy [+1]

Status: Not yet recruiting

Clinical Validation Study on the Imaging Efficacy of Mobile 4D CBCT Technology for Peripheral Pulmonary Lesions

The purpose of this study is to evaluate the clinical value of mobile 4D CBCT technology in the diagnosis and treatment of peripheral pulmonary lesions and to validate its intraoperative dynamic three-dimensional CT imaging capability.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Shanghai Chest HospitalUpdated: Sep 8, 2025Locations: 1
Eligibility criteria

Age >18 years old. [+3]

Contraindications to bronchoscopy are present. [+2]