This study is a prospective, registry trial aimed to compare the clinical and angiographic outcomes of OCT-guided and angiography-guided PCI in patients with coronary DES-ISR.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
240
After randomization, subjects receive primary PCI under the guiding of OCT
After randomization, subjects receive primary PCI under the guiding of angiography
Yundai Chen
Beijing, China
In-segment late loss at 9 months follow-up
Time frame: 9 months
Rates of acute success
Time frame: 1 month
Rate of 9-month binary restenosis
Time frame: 9 months
Number of Participants with target lesion failure (TLF)
Time frame: 12 months
Rate of major adverse cardiovascular events
Time frame: 12 months
Number of participants with all-cause death
Time frame: 12 months
Rate of myocardial infarction
Time frame: 12 months
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