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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04730648
Other study ID # Among-Us study
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 22, 2021
Est. completion date April 23, 2023

Study information

Verified date May 2022
Source Shenzhen People's Hospital
Contact Tangzhiming Li, PhD.
Phone +86 18588269277
Email litangzhiming@126.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Acute coronary syndrome (ACS) is a lethal disease, reduced low-density lipoprotein (LDL) cholesterol due to inhibition of proprotein convertase subtilisin/kexin 9 (PCSK9) reduces cardiovascular events and improve cardiovascular prognosis. we assuming that PCSK9 inhibitor could bring metabolic change in serum, in order to investigate the metabolic modification, we conduct this clinical trial.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date April 23, 2023
Est. primary completion date April 23, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - New diagnosis ACS patient by serum biomarker and coronary arteriography. Exclusion Criteria: - Severe renal dysfunction acute or chronic bacterial and viral infections sleep apnea cancer

Study Design


Intervention

Drug:
PCSK9 inhibitor
For newly diagnosed ACS patients with diabetes, multivessel occlusion, or recurrent ACS attack, who are willing to accept PCSK9 inhibitor injection.

Locations

Country Name City State
China Tangzhiming Li Shenzhen Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Shenzhen People's Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary cardiovascular prognosis composite outcome of time to first occurrence of cardiovascular death, myocardial infarction, unstable angina and heart failure. 52 weeks
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