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A comparative study for EBUS-GS and CT guided percutaneous lung biopsy for the diagnosis of pulmonary occupying lesions

A comparative study for EBUS-GS and CT guided percutaneous lung biopsy for the diagnosis of pulmonary occupying lesions

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900022417
Enrollment
Unknown
Registered
2019-04-10
Start date
2019-04-10
Completion date
Unknown
Last updated
2019-04-15

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

Conditions

pulmonary occupying lessions

Interventions

Gold Standard:CT guided percutaneous lung biopsy
Index test:EBUS-GS&#32
biopsy

Sponsors

General Hospital of Western Theater Command
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: All patients were hospitalized and CT indicated that there were consolidation, mass and exudation in the lungs, which could not be clearly diagnosed by the examination of fiberoptic bronchoscopy, routine sputum and pleural fluid or the diagnostic treatment of anti-inflammatory and anti-tuberculosis. Finally, all patients underwent EBUS-GS and CT guided percutaneous lung biopsy.

Exclusion criteria

Exclusion criteria: All patients received outpatient treatment, or the hospitalized patients who did not undergo percutaneous lung biopsy including those who did not need the lung biopsy, and those who required the lung biopsy to definite diagnosis but the patients and their families refused or there were contraindications to percutaneous lung biopsy.

Design outcomes

Primary

MeasureTime frame
Diagnostic rate;

Secondary

MeasureTime frame
Complications;

Countries

China

Contacts

Public ContactMa Lijie

General Hospital of Western Theater Command

mljp321@163.com+86 18113056825

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026