ClinicalTrials.Veeva

Menu

Determination of Pneumothorax Post Lung Biopsy

University of Minnesota (UMN) logo

University of Minnesota (UMN)

Status

Withdrawn

Conditions

Pneumothorax

Study type

Observational

Funder types

Other

Identifiers

NCT02840032
1606M88672

Details and patient eligibility

About

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

Full 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

Sex

All

Ages

20 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Any lung transplant patient who undergoes to bronchoscopic lung biopsy

Exclusion criteria

  • Patients develop respiratory failure during the procedure

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems