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Clinical Trial Summary

The purpose of this study is to monitor short-term changes in tissue oxygen saturation and local blood flow as results of changing from supine to prone position in ARDS COVID-19 patients


Clinical Trial Description

After obtaining consent to participate in the study, the subjects included in the study will undergo a baseline 15-minute measurement of tissue oxygen saturation (StO2) measured non-invasively on the forearm by means of near-infrared spectroscopy (NIRS). Once a baseline stable StO2 value is obtained, a provocative test, consisting of a transient vascular occlusion, will be performed. The test will allow the obtention of a local metabolic rate, and a StO2 recovery rate after the ischemic stimulus. Tissue oxygenation measurements will be performed in supine position, immediately before changing to prone positioning, and repeated after 20 minutes of stabilization, once in prone position. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04692129
Study type Observational
Source Corporacion Parc Tauli
Contact Jaume Mesquida, MD, PhD
Phone +34 937231010
Email jmesquida@tauli.cat
Status Recruiting
Phase
Start date May 29, 2020
Completion date October 31, 2022

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