Clinical Trials Directory

Trials / Completed

CompletedNCT01068626

Rosuvastatin in Visceral Adiposity

A 26-week, Single Center, Randomized, Placebo-controlled, Double-blind, Parallel-group Study to Evaluate the Effect of Rosuvastatin on Visceral Adipose Tissue in Male Patients With Abdominal Obesity

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
54 (actual)
Sponsor
Göteborg University · Academic / Other
Sex
Male
Age
40 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to investigate whether 6 months treatment with the cholesterol-lowering drug rosuvastatin may reduce visceral fat tissue in obese middle aged men.

Detailed description

The accumulation of intra-abdominal fat has been suggested to be of primary importance in the development of the metabolic syndrome and associated metabolic disturbances and it has been hypothesized that a selective reduction of visceral fat tissue would improve the symptoms of the metabolic syndrome. Treatment with statins decrease levels of LDL-cholesterol and reduce coronary artery disease (CAD) events. Although it is widely accepted that the majority of benefit obtained with statins is a direct result of their lipid-lowering properties, they also demonstrate additional cholesterol-independent or pleiotropic effects. The results of experimental studies have now shown that statins decrease fat mass in the visceral region in an animal model. In the present study, we will investigate whether statins can decrease visceral obesity in humans.

Conditions

Interventions

TypeNameDescription
DRUGRosuvastatin10 mg once daily
DRUGPlacebo for rosuvastatinonce daily

Timeline

Start date
2006-05-01
Primary completion
2008-10-01
Completion
2008-12-01
First posted
2010-02-15
Last updated
2015-08-24
Results posted
2011-03-02

Locations

1 site across 1 country: Sweden

Source: ClinicalTrials.gov record NCT01068626. Inclusion in this directory is not an endorsement.