Clinical Trials Directory

Trials / Completed

CompletedNCT01031667

Synergistic Effect of Combination Therapy With Cilostazol and Probucol on Plaque Stabilization and Lesion Regression: Serial Intravascular Ultrasound and Virtual Histology Study(SECURE Study)

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
118 (actual)
Sponsor
Yonsei University · Academic / Other
Sex
All
Age
20 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the effect of combination therapy with cilostazol and probucol on plaque volume and composition change in comparison with cilostazol alone by serial intravascular ultrasound and virtual histology.

Conditions

Interventions

TypeNameDescription
DRUGCilostazol, Probucol / placebo of probucolAn investigator-initiated, placebo-controlled, randomized, multi-center study. Enrolled patients will be randomized after PCI either to the combination therapy group or to the control group. In the combination therapy group, cilostazol 200 mg and probucol 500 mg will be administered daily, whereas the control group will receive cilostazol 200 mg daily only.

Timeline

Start date
2009-11-01
Primary completion
2011-06-01
Completion
2011-06-01
First posted
2009-12-14
Last updated
2011-06-17

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01031667. Inclusion in this directory is not an endorsement.

Synergistic Effect of Combination Therapy With Cilostazol and Probucol on Plaque Stabilization and Lesion Regression: Se (NCT01031667) · Clinical Trials Directory