Clinical Trials Directory

Trials / Completed

CompletedNCT01043380

Plaque REgression With Cholesterol Absorption Inhibitor or Synthesis Inhibitor Evaluated by IntraVascular UltraSound

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
245 (actual)
Sponsor
Kumamoto University · Academic / Other
Sex
All
Age
30 Years – 85 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study was to evaluate the difference in the effect of coronary plaque regression (as measured by intravascular ultrasound \[IVUS\] imaging) between cholesterol absorption inhibitor and cholesterol synthesis inhibitor.

Conditions

Interventions

TypeNameDescription
DRUGCombination therapy with Lipitor [Atorvastatin] and Zetia [Ezetimibe]Zetia 10 mg/dl + Lipitor. The dosage of Lipitor will be titrated up to a maximum of 20 mg/day with a treatment goal of lowering LDL-C below 70 mg/dl.
DRUGLipitor (Atorvastatin) monotherapyThe dosage will be titrated up to a maximum of 20 mg/day, which is the highest approved regimen by the Ministry of Health, Labor and Welfare of Japan, with a treatment goal of lowering LDL-C below 70 mg/dl.

Timeline

Start date
2010-01-01
Primary completion
2014-03-01
Completion
2014-09-01
First posted
2010-01-06
Last updated
2015-04-01

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT01043380. Inclusion in this directory is not an endorsement.