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Clinical Trial Summary

Bedside ultrasonography for detection of pneumothorax after transbronchial lung biopsies in lung transplant patients


Clinical Trial Description

The patients who undergo transbronchial forceps lung biopsies get a routine CXR after the biopsies are performed. The reason for CXR is to find out if pneumothorax occurred or not. CXR is required patient transportation and interpretation by the radiologist as well as time consuming. Instead, we are planning to perform bedside ultrasound to determine if pneumothorax occurred or not ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02840032
Study type Observational
Source University of Minnesota - Clinical and Translational Science Institute
Contact
Status Withdrawn
Phase
Start date July 2016
Completion date August 2017

See also
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