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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01230294
Other study ID # S275-2010
Secondary ID
Status Active, not recruiting
Phase N/A
First received October 28, 2010
Last updated November 5, 2016
Start date October 2010

Study information

Verified date November 2016
Source Heidelberg University
Contact n/a
Is FDA regulated No
Health authority Germany: Federal Institute for Drugs and Medical Devices
Study type Observational

Clinical Trial Summary

Aims of this study are the evaluation of new echocardiographic methods (3D/4D- and strain-echocardiography) for measurement of the right ventricular (RV) function .


Description:

Studies of the last years revealed that the right ventricular function is an important predictive value for the survival of patients with congenital heart disease, pulmonary hypertension or chronic heart failure. In 2006 the National Heart, Lung and Blood Institute has pronounced the right ventricular dysfunction including the non-invasive assessment of the right ventricular function as preferential aim of cardiovascular research.

Many parameters are used to describe right ventricular dysfunction, but none of these has a comparable significance like the left ventricular ejection fraction. Because of the limitation of each right ventricular parameter the stepwise combination of these parameters is used to describe right ventricular function what frequently results in further problems, especially in comparison of long-term controls.

Aims of this study are the evaluation of new echocardiographic methods (3D/4D- and strain-echocardiography) for measurement of the right ventricular (RV) function. The study is carried out as prospective, monocentric trial at the Department of Cardiology of the University Hospital of Heidelberg. Three different groups are set up for the assessment of the right ventricular function: patients with pulmonary arterial hypertension, patients with chronic heart failure of the left ventricle affecting the right heart and patients without structural heart disease who underwent an echocardiographic examination for other reasons (control group).

All participants are re-examined in constant intervals as clinically indicated.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 150
Est. completion date
Est. primary completion date December 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- persons of 18 years and older who receive a transthoracic echocardiography at our department

- written consent

Exclusion Criteria:

- present atrial fibrillation/flutter

- permanent pacemaker rhythm

- moderate/severe valvular heart disease

- pregnancy

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Locations

Country Name City State
Germany University of Heidelberg Heidelberg Baden-Wuerttemberg

Sponsors (1)

Lead Sponsor Collaborator
Heidelberg University

Country where clinical trial is conducted

Germany, 

References & Publications (1)

Greiner S, André F, Heimisch M, Hess A, Steen H, Katus HA, Mereles D. Non-invasive quantification of right ventricular systolic function by echocardiography: a new semi-automated approach. Clin Res Cardiol. 2013 Mar;102(3):229-35. doi: 10.1007/s00392-012- — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary 3D-volumetry of the right ventricle 2 years No
Primary 2D strain of the right ventricle 2 years No
Secondary pulmonary artery systolic pressure (PASP) standard value: = 30 mmHg 2 years No
Secondary tricuspid annular plane systolic excursion (TAPSE) standard value: = 20 mm 2 years No
Secondary tricuspid annular systolic velocity (TASV) standard value: = 20cm/s 2 years No
Secondary Tei-index (myocardial performance index) standard value: = 0,5 2 years No
Secondary LV-eccentricity-index (Lei-index) standard value: = 1,0 2 years No
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