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Clinical Trial Summary

The purpose of the study is to determine if a protocol that assesses patients' daily fluid intake and output can decrease the overall amount of fluid patients receive during the first five days in the ICU. The study will also determine if decreasing overall fluids can decrease adverse events associated with mechanical ventilation, such as ventilator-associated pneumonias.

The protocol will include daily ultrasounds and blood draws to evaluate fluid balance. Ultrasound will be used to measure changes in the diameter of the inferior vena cava with respiration.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02473718
Study type Interventional
Source Washington University School of Medicine
Contact
Status Completed
Phase N/A
Start date January 2014
Completion date January 2015

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