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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01341730
Other study ID # CUKCVC
Secondary ID
Status Terminated
Phase Phase 4
First received
Last updated
Start date June 2011
Est. completion date August 2012

Study information

Verified date July 2020
Source The Catholic University of Korea
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is a prospective randomized clinical trial and to compare the antiinflammatory effect of atorvastatin single therapy and atorvastatin and pioglitazone combination therapy in carotid arteries of stable and unstable angina patients by PET/CT.


Recruitment information / eligibility

Status Terminated
Enrollment 41
Est. completion date August 2012
Est. primary completion date June 2012
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- The subject who has undergone percutaneous coronary intervention due to coronary artery disease ( stable angina or unstable angina)

- The subject described above who has atherosclerotic plaque in his/her carotid artery by carotid ultrasonography

- The subject who or a legal representative agrees to the clinical trial and gives written permission to the IRB-approved form.

Exclusion Criteria:

- The subjets who have taken statins or thiazolidinedione with 4 weeks

- Marked elevated liver enzyme ( more than 2.5 fold compared to reference range)

- Renal insufficiency patients ( serum creatinine more than 2 mg/dl)

- Congestive heart failure ( NYHA class 2-4)

- Acue myocardial infarction

- Unstable angina with ST segment deviation

- Pregnancy

- The subjects enrolled in another studies

Study Design


Intervention

Drug:
Atorvastatin 20mg
20 mg QD for 3 months
Atorvastatin 20 mg + Pioglitazone 30 mg
atorvastatin 20 mg plus pioglitazone 30 mg QD for 3 months

Locations

Country Name City State
Korea, Republic of Cardiovascular center, Seoul St. Mary's hospital Seoul

Sponsors (2)

Lead Sponsor Collaborator
The Catholic University of Korea Jeil Pharmaceutical Co., Ltd.

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Difference of Standardized Uptake Value (SUV) of Atherosclerotic Plaque in Carotid Artery by PET CT 3 months
Secondary Difference PET CT Parameters in 3 Months Compared to Initial Evaluation Change of Maximum Standardized Uptake Value (SUVmax),Mean Standardized Uptake Value (SUVmean)- no unit for this value 3 months
Secondary Difference of Laboratory Data Compared to Initial Evaluation Change of high sensitivity C-reactive protein (hsCRP, mg/dl) Change of low density lipoprotein cholesterol(mg/dl) Change of high density lipoprotein cholesterol(mg/dl) Change of triglyceride (mg/dl) Change of matrix metalloproteinase 9 (mcg/ml) Change of plasminogen activator inhibitor (PAI)-1 (ng/ml) Change of Homeostatic Model Assessment (HOMA) index (%) 3 months
Secondary Clinical Incidents Major adverse cerebro-cardiovascular event: a composite of cardiac death, nonfatal myocardial infarction, stroke, and target vessel revascularization 3 months
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