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

Aymen N Naguib

Status: Terminated

Conditions: Congenital Heart Disease

Treatments: Device: Regional saturation monitor

Study type: Observational

Funder types: Other

Identifiers

NCT02060825

IRB12-00687

Details and patient eligibility

About

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).

Enrollment: 16 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Diagnosis of single ventricle and undergoing the hybrid procedure pathway.

Exclusion criteria

• None

Trial design

16 participants in 1 patient group

Regional saturation monitor

Description:

Patients undergoing surgical repair of hypoplastic left heart syndrome.

Treatment:

Device: Regional saturation monitor