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The Use of Optical Oximetry in Determining Gastrointestinal Complications After the Hybrid Procedure

Congenital Heart Disease Clinical Trial

Clinical Trial Summary

This project is evaluating the validity of regional saturation monitoring in evaluating changes in the mesenteric perfusion. Regional saturation monitoring is a standard of care in many institutions, including NCH. Advances in the technology and recent approval of the use of CASMED devices for this purpose will allow us to use this technology more effectively. We aim to evaluate if there is a change in the mesenteric blood flow during the pre, intra and post operative period for the hybrid procedure and the balloon atrial septostomy procedure (BAS).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02060825
Study type Observational
Source Nationwide Children's Hospital
Contact
Status Terminated
Phase N/A
Start date November 2012
Completion date September 2016
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