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Clinical trial

A With-in Subject, Controlled Study to Determine the Sensitivity and Specificity of the Cardiox Flow Detection System for the Detection of Right-to-Left Cardiac Shunts Compared to Transesophageal Echocardiography and Transcranial Doppler Ultrasound

NCT01773252 is registered in ClinicalTrials.gov with Cardiox Corporation as lead sponsor.

NCT NCT01773252
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Registry record

As filed in ClinicalTrials.gov.

Title
A With-in Subject, Controlled Study to Determine the Sensitivity and Specificity of the Cardiox Flow Detection System for the Detection of Right-to-Left Cardiac Shunts Compared to Transesophageal Echocardiography and Transcranial Doppler Ultrasound
Lead sponsor
Cardiox Corporation
Phase
Phase 3
Overall status
Terminated
Start date
November 30, 2012
Completion date
November 30, 2015
Enrollment
141 (actual)
Sites
8

Conditions

As the registry lists them; a condition with its own page is linked.

atrial septal defect, patent foramen ovale, right to left shunt