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Clinical Trial Summary

The purpose of this study is to compare cryobiopsies with forceps biopsies during semirigid thoracoscopy.


Clinical Trial Description

The investigators are going to compare diagnostic yield and size, morphological features, immunohistochemistry as measures of the quality of the samples. The secondary aim is to evaluate safety with focus on bleeding intensity. ;


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Diagnostic


Related Conditions & MeSH terms


NCT number NCT01475084
Study type Interventional
Source The University Clinic of Pulmonary and Allergic Diseases Golnik
Contact
Status Completed
Phase Phase 2/Phase 3
Start date November 2011
Completion date November 2014

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