Coronary Artery Disease Clinical Trial
Official title:
Impact of Combined Ezetimibe and Atorvastatin Therapy on Coronary Thin-cap Fibroatheroma As Assessed by Optical Coherence Tomography
After successful coronary angiography and OCT examination, patients with TCFAs in non-culprit, mild-to-moderate stenotic lesions will be enrolled. Then, they will be randomly assigned in a 1:1 ratio to receive either atorvastatin (20 mg/day) alone or atorvastatin (20 mg/day)plus ezetimibe(10 mg/day)by envelope method. Angiographic and OCT follow-up will be scheduled for the target vessel after 12 months.
This is a prospective, randomized , controlled, open-label, single-center study to evaluate
the effect of ezetimibe added to atorvastatin on coronary thin-cap fibroatheroma(TCFA).
After successful coronary angiography and OCT examination, patients with TCFAs in
non-culprit, mild-to-moderate stenotic lesions will be enrolled. Then, they will be randomly
assigned in a 1:1 ratio to receive either atorvastatin (20 mg/day) alone or atorvastatin (20
mg/day)plus ezetimibe(10 mg/day)by envelope method.
Angiographic and OCT follow-up will be scheduled for the target vessel after 12 months.The
primary efficacy endpoint is the change in minimum fibrous cap thickness measured by OCT
from baseline to follow-up.The secondary endpoints include absolute and percent changes in
the lipid, glycemic, and inflammatory profile. Then, changes of these indicators above will
be compared respectively in diabetic and non-diabetic patients.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
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