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Lung and Diaphragm Ultrasound in the Early Postoperative Course Following Lung Transplantation — LUS  

Lung Transplantation Clinical Trial

Official title:
Lung and Diaphragm Ultrasound in the Early Postoperative Course Following Lung Transplantation

Clinical Trial Summary

This feasibility study tries to define the value of daily Lung and Diaphragm Ultrasound in the early postoperative course following Lung transplantation by comparing its diagnostic accuracy with that of standard of care diagnostic procedures

Clinical Trial Description

Lung transplantation remains a high risk procedure. Common complications in the early postoperative course are, among others, primary graft dysfunction (PGD), hemorrhage, anastomosis insufficiency leading to pneumothorax, pneumonia, atelectasis and diaphragm dysfunction. Early diagnosis of complications is important to avoid further deterioration. Lung ultrasound (LUS) and diaphragm ultrasound (DUS) has a high diagnostic accuracy for identifying frequent conditions in the critically ill. Studies evaluating its value in patients following lung transplantation are missing. This study investigates the feasibility and clinical ability of LUS and DUS to identify common complications following lung transplantation and compares it to standard of care diagnostic procedures. The investigators start a prospective cohort study of lung transplant recipients who undergo lung transplantation at the university hospital Munich. Daily LUS and DUS in the early postoperative phase will be performed to detect and monitor complications. The US results will be compared to the results of diagnostic procedures of the clinical routine such as clinical examination, chest x ray, hemodynamic monitoring, expert opinion on PGD and laboratory parameters. The hypothesis is that daily LUS and DUS following lung transplantation helps to diagnose complications early and with higher accuracy compared to the results of diagnostic procedures of the clinical routine. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04891094
Study type Interventional
Source Ludwig-Maximilians - University of Munich
Contact
Status Completed
Phase N/A
Start date April 16, 2021
Completion date May 15, 2022
View Details
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