Clonidine and Left Ventricular Dysfunction

This study has been withdrawn prior to recruitment.

First Received: September 13, 2005 Last Updated: November 28, 2007 History of Changes

Sponsored by:	University Hospital, Strasbourg, France
Information provided by:	University Hospital, Strasbourg, France
ClinicalTrials.gov Identifier:	NCT00213902

Purpose

The objectives of this study are:

To evaluate the effect of clonidine, a sympathetic modulator, to reverse cardiac remodeling and to improve hemodynamics in diastolic heart failure (DHF).
To evaluate the effect of clonidine on neurohormones and quality of life in patients with DHF.

The study is a double-blind, placebo-controlled study evaluating the effects of clonidine compared to placebo in patients with DHF. A total of 70 patients with DHF will be randomized in a 1:1 ratio to:

placebo (n=35) or to
clonidine (n=35) in a dose of 0.075 mg twice a day for the first 6 weeks followed by uptitration to 0.150 mg twice a day for 6 months.

The primary outcome is the reversion of cardiac remodeling and hemodynamic parameters evaluated by magnetic resonance imaging (MRI) and echocardiography.

Condition	Phase
Ventricular Dysfunction	Phase II

MedlinePlus related topics: Heart Failure

Drug Information available for: Clonidine

U.S. FDA Resources

Study Type:	Observational
Study Design:	Prospective
Official Title:	Evaluation of Effects of Central Sympathetic Inhibition in Elderly With Left Ventricular Diastolic Dysfunction and Preserved Ejection Fraction: A Proof-of-Concept Trial With Clonidine

Further study details as provided by University Hospital, Strasbourg, France:

Estimated Enrollment:	70
Study Start Date:	April 2004

Eligibility

Ages Eligible for Study:	60 Years and older
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

Age: 60 and greater
Gender: Both
Patients with heart failure New York Heart Association (NYHA) II and ejection fraction over 45%

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00213902

Sponsors and Collaborators

University Hospital, Strasbourg, France

Investigators

Principal Investigator:

Pascal Bousquet, MD

Hopitaux Universitaires de Strasbourg

More Information

No publications provided

Study ID Numbers:	3153
Study First Received:	September 13, 2005
Last Updated:	November 28, 2007
ClinicalTrials.gov Identifier:	NCT00213902 History of Changes
Health Authority:	France: Afssaps - French Health Products Safety Agency

Keywords provided by University Hospital, Strasbourg, France:

Heart failure
Diastolic
functionClonidine
Left ventricular diastolic dysfunction with preserved ejection fraction

Study placed in the following topic categories:

Ventricular Dysfunction
Heart Failure
Heart Diseases
Clonidine
Ventricular Dysfunction, Left

Additional relevant MeSH terms:

Ventricular Dysfunction
Heart Diseases
Ventricular Dysfunction, Left
Cardiovascular Diseases

ClinicalTrials.gov processed this record on May 07, 2009