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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01174680
Other study ID # CGM@CAD
Secondary ID
Status Completed
Phase N/A
First received June 7, 2010
Last updated March 13, 2017
Start date December 2010
Est. completion date April 2011

Study information

Verified date August 2010
Source Stiftung Institut fuer Herzinfarktforschung
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 43
Est. completion date April 2011
Est. primary completion date February 2011
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Stiftung Institut fuer Herzinfarktforschung

Outcome

Type Measure Description Time frame Safety issue
Primary additional value of cardiogoniometry 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. at hospital admission
Primary additional value of cardiogoniometry 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. at hospital discharge
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