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Effects of Endurance Training on Patients With Reduced Left Ventricular Ejection Fraction (LVEF) and Cardiac Resynchronisation Therapy Especially for Cardiac Arrhythmias

The recruitment status of this study is unknown because the information has not been verified recently.
Verified May 2007 by Charite University, Berlin, Germany.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
Charite University, Berlin, Germany
ClinicalTrials.gov Identifier:
NCT00472238
First received: May 10, 2007
Last updated: November 19, 2008
Last verified: May 2007

May 10, 2007
November 19, 2008
August 2007
Not Provided
  • left ventricular function [ Time Frame: 3 months ]
  • aerobic threshold [ Time Frame: 3 months ]
Not Provided
Complete list of historical versions of study NCT00472238 on ClinicalTrials.gov Archive Site
quality of life [ Time Frame: 3 months ]
Not Provided
Not Provided
Not Provided
 
Effects of Endurance Training on Patients With Reduced Left Ventricular Ejection Fraction (LVEF) and Cardiac Resynchronisation Therapy Especially for Cardiac Arrhythmias
Effects of Endurance Training on Patients With Reduced LVEF and Cardiac Resynchronisation Therapy Especially for Cardiac Arrhythmias

A severely reduced left ventricular ejection fraction is associated with increased mortality due to pump failure as well as to malignant ventricular arrhythmia. We hypothesize that targeted training may lead to improved survival and to increased parameters of risk stratification for malignant arrhythmia. Additionally, the training may lead to an improved psychological and mental condition of the patients

Not Provided
Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Heart Failure
  • Cardiac Resynchronisation Therapy
  • Sudden Cardiac Death
  • Behavioral: endurance training
    control group.
  • Behavioral: exercise training
    Treadmill exercise training to optimize physical endurance
  • Experimental: 1, Training
    Group for training therapy
    Intervention: Behavioral: exercise training
  • Active Comparator: 2, Control
    Intervention: Behavioral: endurance training
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
30
December 2008
Not Provided

Inclusion Criteria:

  • CRT Device

Exclusion Criteria:

  • refused informed consent
Both
18 Years to 80 Years
No
Germany
 
NCT00472238
CBF-2007001, 001
Yes
Dr. Dirk Müller, Charité Campus Benjamin Franklin
Charite University, Berlin, Germany
Not Provided
Principal Investigator: Dirk Müller, MD, PhD Charité, Campus Benjamin Franklin
Principal Investigator: Fernando C Dimeo, MD, PhD Charité, Campus Benjamin Franklin
Charite University, Berlin, Germany
May 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP