Actively Recruiting
A Longitudinal Cohort of Patients With Acute Coronary Syndrome Undergoing Percutaneous Coronary Intervention
Led by Su Guohai · Updated on 2023-02-09
10000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
S
Su Guohai
Lead Sponsor
S
Shandong First Medical University
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are studying patients with acute coronary syndrome who undergo percutaneous coronary intervention to understand the risk factors that affect the occurrence and prognosis of this condition. This observational study will follow participants for at least two years to track major adverse cardiovascular events, including all-cause mortality, cardiovascular mortality, and ischemic stroke. The study is led by Su Guohai and aims to gather comprehensive data to improve knowledge about acute coronary syndrome outcomes. Participants will have blood and fecal samples collected for detailed analysis. Clinical information such as diagnosis, medical history, lab test results, treatment methods, prognosis, and follow-up data will also be recorded. The study focuses on monitoring the progression and outcomes of acute coronary syndrome over time through regular data collection. During the study, participants will be closely followed up to document any major cardiovascular events over a two-year period and beyond. Researchers will assess various health measures and risk factors to better understand how acute coronary syndrome develops and progresses. The total duration of participation includes initial enrollment and ongoing observation to capture long-term outcomes.
CONDITIONS
Brief Title
A Cohort of Patients Undergoing Percutaneous Coronary Intervention
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with acute coronary syndrome and scheduled to undergo percutaneous coronary intervention
- Aged over 18 years
You will not qualify if you...
- Having malignant tumors, acute infectious diseases, or advanced liver diseases
- Not willing to sign an informed consent form
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 1 week
Participants undergo percutaneous coronary intervention and related diagnostic assessments.
1 visit (in-person)
Duration - Up to 2 years
Participants are followed up to monitor for major adverse cardiovascular events and other health outcomes. Blood and fecal samples are collected for further analysis along with clinical information.
Periodic visits over 2 years
Trial Site Locations
Total: 1 location
1
Jinan Central Hospital
Jinan, Shandong, China
Actively Recruiting
Research Team
G
Guohai Su, doctor
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here