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Terminated Phase 3 Interventional

Cardiox Shunt Detection Technology Study

ClinicalTrials.gov ID: NCT01333761

Public ClinicalTrials.gov record NCT01333761. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 2:15 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

FDS-0004 Cardiox Shunt Detection Technology Study

Study identification

NCT ID
NCT01333761
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Cardiox Corporation
Industry
Enrollment
71 participants

Conditions and interventions

Interventions

  • Cardiox FDS Device

Device

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 31, 2011
Primary completion
Jun 30, 2012
Completion
Jun 30, 2012
Last update posted
Jan 8, 2013

2011 – 2012

United States locations

U.S. sites
7
U.S. states
7
U.S. cities
7
Facility City State ZIP Site status
University of Alabama, Birmingham Birmingham Alabama 35249
Heart and Vascular Center of Arizona Phoenix Arizona 85006
UCLA Medical Center Los Angeles California 90095
Tufts Medical Center Boston Massachusetts 02111
Columbia University Medical Center New York New York 10032
Riverside Methodist Hospital Columbus Ohio 43214
Swedish Hospital Seattle Washington 98122

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01333761, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 8, 2013 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01333761 live on ClinicalTrials.gov.

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