Clinical Trials Directory

Trials / Unknown

UnknownNCT00669435

Losartan and Simvastatin in Hypertensive Obeses With Liver Steatosis

Ultrasonographic Modification of Liver Steatosis and Visceral Fat Induced by Treatment With Losartan and Simvastatin in Hypertensive Normocholesterolemic Obese Patients

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
75 (estimated)
Sponsor
University of Pavia · Academic / Other
Sex
All
Age
40 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Angiotensin II has been proposed as a lipid metabolism regulator. It is known that adipocytes secrete a variety of protein, such as TNFα, plasminogen activator inhibitor (PAI)-1, leptin, resistin and adiponectin; these proteins have a wide range of biological effects and are associated with insulin resistance. Adipocytes also produce angiotensinogen and angiotensin II and a local renin-angiotensin system (RAS) is present in adipose tissue. In overweight or obese hypertensive normocholesterolemic patients the treatment with AT1-receptor blocker (Losartan) may have a better effect on hepatic steatosis and visceral fat deposition than the antihypertensive treatment with calcium channel blocker (amlodipine). Simvastatin will be added to both groups. The aim of this study is to evaluate the effect of losartan and simvastatin on ultrasonographic qualitative and quantitative parameters in overweight or obese hypertensive normocholesterolemic patients with hepatic steatosis.

Conditions

Interventions

TypeNameDescription
DRUGLosartan + Simvastatintablets; 50, 100 mg; od; 12 months tablets; 20 mg; od; 6 months
DRUGAmlodipine + Simvastatintablets; 5, 10 mg; od; 12 months tablets; 20 mg; od; 6 months

Timeline

Start date
2008-04-01
Primary completion
2008-04-01
Completion
2009-04-01
First posted
2008-04-30
Last updated
2008-04-30

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT00669435. Inclusion in this directory is not an endorsement.