Clinical Trials Directory

Trials / Terminated

TerminatedNCT02060825

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

Status
Terminated
Phase
Study type
Observational
Enrollment
16 (actual)
Sponsor
Aymen N Naguib · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

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).

Conditions

Interventions

TypeNameDescription
DEVICERegional saturation monitor

Timeline

Start date
2012-11-01
Primary completion
2016-09-01
Completion
2016-09-01
First posted
2014-02-12
Last updated
2017-02-01

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02060825. Inclusion in this directory is not an endorsement.