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

NCT02060825 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 16

Last updated 2017-02-01

No results posted yet for this study

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

  • Congenital Heart Disease

Interventions

DEVICE

Regional saturation monitor

Sponsors & Collaborators

  • Aymen N Naguib

    lead OTHER

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-11-30
Primary Completion
2016-09-30
Completion
2016-09-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02060825 on ClinicalTrials.gov