Loading clinical trials...
Loading clinical trials...
This is a multi-center, randomized controlled study to investigate whether early offering PCSK9 inhibitor can protect against negative inflammatory response and organ dysfunction after coronary artery bypass grafting (CABG). Subjects with myocardial ischaemic syndromes (MIS) will be enrolled in this study after consent information. After randomization, the control group will receive standard therapy, while the experiment group will receive first PCSK9 inhibitor before CABG, then twice a month until 3 months later. Six month after CABG, CRP will be used to evaluate inflammation, and echocardiography and coronary CTA will be used to evaluate cardiovascular function.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Beijing Anzhen Hospital, Capital Medical University
Beijing, Beijing Municipality, China
The First Affiliated Hospital of Nanjing Medical University
Nanjing, Jiangsu, China
Start Date
January 1, 2025
Primary Completion Date
December 31, 2026
Completion Date
December 31, 2026
Last Updated
December 12, 2024
400
ESTIMATED participants
PCSK9 inhibitor
DRUG
Statin
DRUG
Lead Sponsor
Nanjing Medical University
Collaborators
NCT06216847
NCT07149688
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06759805