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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05159804
Other study ID # CPL-2017
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date January 1, 2017
Est. completion date December 30, 2030

Study information

Verified date December 2021
Source Changhai Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This multicenter study involved 5 hospitals (Changhai Hospital; Yueyang Hospital of Shanghai University of Traditional Chinese Medicine; Gongli Hospital; Putuo Hospital of Shanghai University of Traditional Chinese Medicine; No. 904 Hospital of the PLA Joint Logistics Support Force Wuxi). The study enrolled 3637 patients with coronary atherosclerosis who were confirmed by coronary angiography from January 2017 through December 2018.


Description:

Patients with coronary atherosclerosis who were confirmed by coronary angiography were eligible for the study. Carotid ultrasonography was simultaneously performed, and carotid intima-media thickness (IMT), maximum thickness and length of all plaques were measured.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 3637
Est. completion date December 30, 2030
Est. primary completion date June 30, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients=18 years old, those who underwent carotid ultrasonography and first coronary angiography simultaneously. Exclusion Criteria: - Patients with known coronary artery disease, previous coronary or carotid revascularization, missing carotid ultrasound or coronary angiography results.

Study Design


Locations

Country Name City State
China Changhai Hospital Shanghai Shanghai
China Gongli Hospital Shanghai Shanghai
China Putuo Hospital Shanghai Shanghai
China Yueyang Hospital Shanghai Shanghai
China No. 904 Hospital of the PLA Joint Logistics Support Force Wuxi Jiangsu

Sponsors (5)

Lead Sponsor Collaborator
Changhai Hospital Gongli Hospital, No. 904 Hospital of the PLA Joint Logistics Support Force, Putuo Hospital, Shanghai University of Traditional Chinese Medicine, Yueyang Hospital, Shanghai University of Traditional Chinese medicine

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Major adverse cardiovascular events A composite of cardiovascular death, myocardial infarction, and stroke 3 years
Secondary Incident cardiovascular events A composite of cardiovascular death, myocardial infarction, stroke, and unplanned coronary artery revascularization 3 years
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