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Clinical Trial Summary

The aim of this study is to assess the capability of a modified under bed weighing scale (contact-free unconstrained respiratory monitor, BSS) to predict postoperative pulmonary complications in high-risk surgical patients. The study is designed to test the hypothesis that abnormal breathing measured by a modified under bed weighing scale predicts postoperative pulmonary complications within 7 days after surgery.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04736212
Study type Observational
Source Beth Israel Deaconess Medical Center
Contact
Status Completed
Phase
Start date March 24, 2021
Completion date April 1, 2022

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