Cardiogoniometry for Early Diagnosis of Coronary Artery Disease Symptomatik

Sponsor

Stiftung Institut fuer Herzinfarktforschung (Other)

Overall Status

Completed

CT.gov ID

NCT01174680

Collaborator

(none)

Enrollment

Arm

Actual Duration (Months)

Study Details

Study Description

Brief Summary

The register study CGM@CAD will examine whether cardiogoniometry can provide additional information concerning the indication for a diagnostic coronary angiography and if so, which additional value it has. Therefore, an additional cardiogoniometry will be carried out in consecutive patients who have been diagnosed with myocardial ischemia by means of established methods (exercise ECG, stress echocardiography, myocardial scintigraphy, or stress-MRT) and for whom an intracardiac catheter examination is regarded as indicated. The results of the different methods - particularly the results of the exercise ECG and the cardiogoniometry - will be checked against the results of the invasive examination as gold standard and the discharge diagnosis with regards to any correlation.

Condition or Disease	Intervention/Treatment	Phase
Stable Angina Pectoris	Procedure: cardiogoniometry	N/A

Study Design

Study Type:

Interventional

Actual Enrollment :

43 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Diagnostic

Official Title:

Cardiogoniometry Zur Früherkennung CAD Symptomatik

Actual Study Start Date :

Dec 1, 2010

Actual Primary Completion Date :

Feb 1, 2011

Actual Study Completion Date :

Apr 1, 2011

Arms and Interventions

Arm	Intervention/Treatment
Experimental: patients with stable angina pectoris stable patients, who have been admitted to one of the participating centres for an elective coronary angiography	Procedure: cardiogoniometry In the course of the project a cardiogoniometry will be carried out during the ambulant or residential hospitalization before the coronary angiography.

Arm

Intervention/Treatment

Experimental: patients with stable angina pectoris

stable patients, who have been admitted to one of the participating centres for an elective coronary angiography

Procedure: cardiogoniometry

In the course of the project a cardiogoniometry will be carried out during the ambulant or residential hospitalization before the coronary angiography.

Outcome Measures

Primary Outcome Measures

additional value of cardiogoniometry [at hospital admission]
The protocol defines that the medical examination is to be preformed at hospital adimssion and again at discharge. Aim is to examine if cardiogoniometry can provide additional information for the decision to perform a diagnostic coronary angiography and if so, which additional value it has.
additional value of cardiogoniometry [at hospital discharge]
The protocol defines that the medical examination is to be preformed at hospital adimssion and again at discharge. Aim is to examine if cardiogoniometry can provide additional information for the decision to perform a diagnostic coronary angiography and if so, which additional value it has.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Indication for a coronary angiography
Age > 18 years
Patients written informed consent

Exclusion Criteria:

Patients with known CHD (condition after myocardial infarction and/or angio-graphically proven stenosis > 50% and/ or revascularization )
Patients with acute coronary syndrome
Patients with pace maker
Severe valvular heart defect
50% extrasystole
Patients with dysrhythmia, which make a correct interpretation impossible (e.g. VES, bigeminies and other dysrhythmia with a high impact such as atrial extrasystoles)
Branch block
Atrial fibrillation

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

Stiftung Institut fuer Herzinfarktforschung

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

Stiftung Institut fuer Herzinfarktforschung

ClinicalTrials.gov Identifier:

NCT01174680

Other Study ID Numbers:

CGM@CAD

First Posted:

Aug 4, 2010

Last Update Posted:

Mar 14, 2017

Last Verified:

Aug 1, 2010

Keywords provided by Stiftung Institut fuer Herzinfarktforschung

cardiogoniometry

stable angina pectoris patients

Additional relevant MeSH terms:

Angina Pectoris

Angina, Stable

Study Results

No Results Posted as of Mar 14, 2017