Clinical Evaluation of the CADence Device in Detection of Coronary Artery Diseases

CompletedOBSERVATIONAL
Enrollment

1,014

Participants

Timeline

Start Date

June 14, 2013

Primary Completion Date

February 10, 2016

Study Completion Date

February 10, 2016

Conditions
Coronary Artery Disease
Interventions
DIAGNOSTIC_TEST

CADence

"Patients with chest pain and two or more coronary risk factors and who were already indicated for nuclear stress test were enrolled in the study. The CADence was performed prior to nuclear stress test. Patients underwent standard angiogram based upon normal clinical judgement. In all other patients a CT angiogram followed.~CADence is a handheld equipped with acoustic sensor technology, a patient booklet, remote algorithm and final report."

Trial Locations (24)

10032

Columbia University, New York

Mt. Sinai, New York

17602

Lancaster General, Lancaster

20010

MedStar Washington Hospital Center, Washington D.C.

21218

MedStar Union Memorial Hospital, Baltimore

33756

Clearwater Cardiovascular, Clearwater

35294

University of Alabama, Birmingham

35801

Heart Center Research, LLC, Huntsville

36608

Cardiology Associates of Mobile, Mobile

38301

Jackson Clinic, Jackson

44035

North Ohio Research, Elyria

48202

Henry Ford Hospital, Detroit

50314

Iowa Heart Center, Des Moines

55102

HealthEast - St. Joseph's Hospital, Saint Paul

United Heart and Vascular Clinic, Saint Paul

55433

Mercy Hospital, Coon Rapids

55455

Abbott/Minneapolis Heart Institute, Minneapolis

University of Minnesota, Minneapolis

55905

Mayo Clinic, Rochester

56303

CentraCare Heart & Vascular Center, Saint Cloud

63141

Mercy Hospital St. Louis, St Louis

90502

UCLA, Los Angeles

06102

Hartford Hospital, Hartford

07666

Holy Name Medical Center, Teaneck

Sponsors
All Listed Sponsors
lead

AUM Cardiovascular, Inc.

INDUSTRY