Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06962436

RAB Versus Ultrathin Bronchoscopy With VBN in the Diagnosis of PPNs

Led by Shanghai Chest Hospital · Updated on 2026-03-25

186

Participants Needed

5

Research Sites

73 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to evaluate whether the diagnostic yield of robotic-assisted bronchoscopy is not inferior to that of the virtual bronchoscopic navigation combined with ultrathin bronchoscopy.

CONDITIONS

Official Title

RAB Versus Ultrathin Bronchoscopy With VBN in the Diagnosis of PPNs

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older, any gender
  • Presence of peripheral lung nodules suspected of malignancy on chest CT requiring non-surgical biopsy
  • Voluntarily agree to undergo bronchoscopy and meet bronchoscopy requirements
  • Understand the study purpose, comply with exams and follow-ups, and provide informed consent
Not Eligible

You will not qualify if you...

  • Contraindications for bronchoscopy such as active massive bleeding, recent heart attack or unstable angina, severe heart or lung dysfunction, severe hypertension or arrhythmias, uncorrectable bleeding disorders, uremia, severe pulmonary artery hypertension, severe superior vena cava syndrome, intracranial hypertension, acute stroke, aortic dissection or aneurysm, multiple bullae, or extreme systemic exhaustion
  • Presence of pure ground-glass nodules suspected of malignancy on chest CT
  • Breastfeeding, pregnant, or planning pregnancy in female patients
  • Having electromagnetic active implantable medical devices
  • Allergy to anesthetics or history of severe allergies or hereditary allergies
  • Participation in drug clinical trials within 3 months or medical device trials within 30 days prior to screening
  • Any other condition the investigator considers unsuitable for participation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 5 locations

1

Shandong Public Health Clinical Center

Jinan, Shandong, China, 250000

Actively Recruiting

2

Ruijin Hospital, Shanghai Jiao Tong University School of Medicine

Shanghai, Shanghai Municipality, China, 200025

Actively Recruiting

3

Shanghai Chest Hospital

Shanghai, Shanghai Municipality, China, 200030

Actively Recruiting

4

Zhongshan Hospital,Fudan University

Shanghai, Shanghai Municipality, China, 200032

Actively Recruiting

5

Sir Run Run Shaw Hospital , affiliated with the Zhejiang University School of Medicine

Hangzhou, Zhejiang, China, 310016

Actively Recruiting

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Research Team

X

Xiaoxuan Zheng

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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