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A Comparative Study of Radial Endobronchial Ultrasound-Guided Transbronchial Cryobiopsy versus Forceps Biopsy in the Diagnosis of Solitary Pulmonary Nodules

A Comparative Study of Radial Endobronchial Ultrasound-Guided Transbronchial Cryobiopsy versus Forceps Biopsy in the Diagnosis of Solitary Pulmonary Nodules

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122727
Enrollment
Unknown
Registered
2026-04-16
Start date
2026-04-16
Completion date
Unknown
Last updated
2026-04-20

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

Conditions

lung cancer, pulmonary sarcoidosis, infectious pulmonary nodules, pulmonary tuberculosis, pneumoconiosis nodules, etc

Interventions

matched historical cohort group:forceps biopsy
intervention group:Transbronchial pulmonary cryobiopsy

Sponsors

Chui Yang Liu Hospital affiliated to Tsinghua University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Thin-section CT indicates peripheral solitary pulmonary nodules (diameter < 30mm), with negative results from conventional bronchoscopy (without navigation/ultrasound guidance); 2.The patient or their legal representative has signed the informed consent form; 3.The expected survival period is more than 6 months, and the patient can cooperate with the 6-month follow-up.

Exclusion criteria

Exclusion criteria: 1.Intolerance to intravenous anesthesia or bronchoscopic procedures (e.g., severe cardiopulmonary insufficiency); 2.severe arrhythmia (e.g., uncontrolled ventricular tachycardia); 3.Coagulation disorders (INR > 1.5 or platelets 100 ml within 24 hours); 4.Nodules adjacent to large blood vessels (distance < 5 mm) or pleura (distance < 2 mm), with extremely high biopsy risk evaluated by multidisciplinary consultation (MDC); 5.Complicated with severe infection, immunodeficiency, or advanced malignant tumors.

Design outcomes

Primary

MeasureTime frame
diagnostic rate;

Secondary

MeasureTime frame
Biopsy time(minutes);The proportion of specimens adequate for genetic testing;Percentage of specimens =2mm in diameter;bleeding;pneumothorax;subgroup diagnostic rate;

Countries

China

Contacts

Public ContactChen Xing

Chui Yang Liu Hospital affiliated to Tsinghua University

chx1020@163.com+86 10 87746704

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 23, 2026