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Clinical Trial Summary

The objective of this study is comparing the attributable procedural time of Endobronchial Ultrasound - Transbronchial Needle Aspiration (EBUS-TBNA) when sampling mediastinal and hilar lymph nodes with or without Rapid On-Site Evaluation (ROSE). The primary outcome will be the time elapsed from EBUS bronchoscope insertion to bronchoscope withdrawal. Secondary outcomes will include total number of sampled lymph nodes, average number of needle aspirations per lymph node sampled, overall diagnostic yield, and procedural time of the cytopathologist.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Benign and Malignant Mediastinal and Hilar Lymph Nodes Known or Suspected Malignancy
  • ENDOBRONCHIAL ULTRASOUND - TRANSBRONCHIAL NEEDLE ASPIRATION

NCT number NCT02028052
Study type Interventional
Source Duke University
Contact
Status Terminated
Phase N/A
Start date April 2012
Completion date November 2014