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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04416425
Other study ID # ZiboCH
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date July 30, 2021
Est. completion date February 27, 2023

Study information

Verified date May 2020
Source Zibo Central Hospital
Contact Bo Li, Doctor
Phone +86-18560292371
Email libosubmit@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Compelling evidences indicate that lipid-lowering therapy can reduce the high-risk plaque feathers and improve the coronary flow reserve. This study is going to investigate the change of lesion-specific hemodynamic significance as determined by ML(Machine Learning)-based CT-FFR (Computed Tomography-Fractional Flow Reserve)after Evolocumab treatment.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 200
Est. completion date February 27, 2023
Est. primary completion date December 31, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: - 1.baseline CCTA revealed at least one lesion with stenotic extent from 50% to 69% on major epicardial arteries (diameter ?2 mm); - 2.patients were referred for optimal medical treatment; - 3.patients agreed to undergo follow-up CCTA at 1-year interval. Exclusion Criteria: - 1.patients had previous history of myocardial infarction or coronary revascularization; - 2.patients were contraindicated to the usage of iodine contrast media; - 3.image quality of baseline or follow-up CCTA was severely impaired (in presence of severe artifact, non-diagnostic); - 4.patients withdrew the informed consents during follow-up; - 5.patients experienced major adverse cardiac events during follow-up; - 6.patients refused to undergo follow-up CCTA; - 7.lost follow-up

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Zibo Central Hospital Zibo Shandong

Sponsors (1)

Lead Sponsor Collaborator
Zibo Central Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Other the change of minimal lumen diameter between baseline and follow-up CCTA After one year's treatment of Elovocumab Injection, the patients will undergo follow-up CCTA again. We will measure the minimal lumen diameter for each lesion. Minimal lumen diameter will be manually measured with a digital caliper at the narrowest level of the lesion using the crosssectional images accroding to the CCTA findings. The results of the minimal lumen diameter at baseline will be compared with results obtained during follow-up to examine the effects of Elovocumab Injection therapy. June 2020 to December 2021
Other the change of total plaque volume (TPV) between baseline and follow-up CCTA After one year's treatment of Elovocumab Injection, the patients will undergo follow-up CCTA again. We will measure TPV for each lesion. Total plaque volume will be automatically measured using the dedicated plaque analysis software. The results of TPV at baseline will be compared with results obtained during follow-up to examine the effects of Elovocumab Injection therapy. June 2020 to December 2021
Other the change of lesion length between baseline and follow-up CCTA After one year's treatment of Elovocumab Injection, the patients will undergo follow-up CCTA again. The length of lesion at baseline will be compared with results obtained during follow-up to examine the effects of Elovocumab Injection therapy. June 2020 to December 2021
Primary the change of lesion-specific CT-FFR After one year's treatment of Elovocumab Injection, the patients will undergo follow-up CCTA again. We will measure the proximal and distal CT-FFR for each lesion.At the same time ,we will calculated the change in CT-FFR value across the lesion(?CT-FFR=CT-FFRproximal-CT-FFRdistal).To compare the parameters above,we shall identify whether the treatment of Elovocumab Injection improves the lesion-specific CT-FFR. June 2020 to December 2021
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