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
| Type | Name | Description |
|---|---|---|
| DRUG | Combination 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. |
| DRUG | Lipitor (Atorvastatin) monotherapy | The 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.