Compuflo Instrument for Thoracic ES Identification

Status Terminated

Clinical Trial Summary

The purpose of this pilot study is to evaluate whether the Compuflo Epidural Instrument injection pump technology, which is FDA approved for lumbar epidural anesthesia, is also capable of identifying the thoracic epidural space through measurement of pressure levels. While this device is approved by the FDA for use in the procedure of the lumbar epidural, it is not used to perform the epidural procedure but rather to measure the epidural pressure. This study will likewise measure the epidural pressure.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03376256
Study type	Interventional
Source	University of Miami
Contact
Status	Terminated
Phase	N/A
Start date	July 11, 2018
Completion date	July 17, 2018

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