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Effects of Pioglitazone Treatment on Sympathetic Nervous System Function in the Metabolic Syndrome
This study is not yet open for participant recruitment.
Study NCT00408850   Information provided by Baker Heart Research Institute
First Received: December 6, 2006   Last Updated: October 30, 2007   History of Changes

December 6, 2006
October 30, 2007
January 2008
 
Sympathetic nervous system activity, measured as muscle sympathetic nervous activity and whole-body noradrenaline spillover
Same as current
Complete list of historical versions of study NCT00408850 on ClinicalTrials.gov Archive Site
Baroreflex function, adrenoceptor expression
Same as current
 
Effects of Pioglitazone Treatment on Sympathetic Nervous System Function in the Metabolic Syndrome
Mechanisms of Sympathetic Overactivity in the Metabolic Syndrome: Effects of Reversing Insulin Resistance by Drug Treatment

An abdominal distribution of fat is associated with the greatest heart disease risk, because commonly, several risk factors of metabolic origin cluster in these individuals. When this occurs the condition is called the 'metabolic syndrome'.

Increased activity of the sympathetic nervous system resulting in enhanced release of the stress hormone 'noradrenaline', may be one mechanism by which adverse cardiovascular and metabolic sequela of the metabolic syndrome might be mediated. Impaired insulin action may be one factor contributing to increased noradrenaline release.

The aim of this Study is to determine whether treatment with a drug called pioglitazone which is known to improve insulin action, results in reduced sympathetic nervous system activity and stress hormone release when compared to treatment with a dummy drug (placebo).

The rapidly growing burden of obesity together with a population that is becoming older raises the importance of effective strategies for the primary prevention and treatment of the metabolic syndrome in order to combat the epidemic of type 2 diabetes and to reduce the increased risk of cardiovascular mortality.

Increased sympathetic nervous system activity may participate in the pathogenesis and complications of the metabolic syndrome. This Study will use a randomised controlled design to evaluate the effects of pioglitazone treatment on sympathetic activity in middle-aged subjects with the metabolic syndrome.The results will generate new information on the neuroadrenergic effects of thiazolidinediones in this clinical setting. This is relevant to the understanding of the pathophysiology of the metabolic syndrome and to its clinical management.

Phase III
Interventional
Treatment, Randomized, Double Blind (Subject, Investigator), Placebo Control, Parallel Assignment, Efficacy Study
Metabolic Syndrome
Drug: Rosiglitazone
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Not yet recruiting
44
December 2008
 

Inclusion Criteria:

  • Males and females aged 45-65 years,
  • non-smokers,
  • HOMA index > 2.5 and
  • who meet ATP III criteria for the metabolic syndrome

Exclusion Criteria:

  • History of diabetes,
  • previous MI, stroke, heart failure, impaired hepatic or renal function.
  • Inability to cease medications which may affect study parameters.
Both
45 Years to 65 Years
No
Contact: Nora E Straznicky, PhD, MPH 61 3 8532 1371 Nora.Straznicky@baker.edu.au
Australia
 
NCT00408850
 
G 06M 2610
Baker Heart Research Institute
National Heart Foundation, Australia
Principal Investigator: Nora E Straznicky, PhD, MPH Baker Heart Research Institute
Baker Heart Research Institute
October 2007

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