Investigating risk factors in patients with acute coronary syndrome undergoing a procedure
A Longitudinal Cohort of Patients With Acute Coronary Syndrome Undergoing Percutaneous Coronary Intervention
This study is trying to find out what risk factors affect patients with acute coronary syndrome who are having a heart procedure and how these factors relate to their health outcomes over two years.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 10000 (estimated) |
| Ages | 18 Years to 85 Years |
| Sex | All |
| Sponsor | Jinan Central Hospital Academic / other |
| Locations | 1 site (Jinan, Shandong) |
| Trial ID | NCT05719545 on ClinicalTrials.gov |
What this trial studies
This observational study aims to recruit patients diagnosed with acute coronary syndrome who are undergoing percutaneous coronary intervention. Participants will be followed for at least two years to monitor the incidence of major adverse cardiovascular events, including mortality and ischemic stroke. Blood and fecal samples will be collected for further analysis, alongside comprehensive clinical data such as medical history and treatment methods. The study seeks to identify risk factors that influence the occurrence and prognosis of acute coronary syndrome.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 years old diagnosed with acute coronary syndrome requiring percutaneous coronary intervention.
Not a fit: Patients with malignant tumors, acute infectious diseases, advanced liver diseases, or those unwilling to provide informed consent may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved understanding and management of risk factors in patients with acute coronary syndrome, potentially reducing adverse cardiovascular events.
How similar studies have performed: Other studies investigating risk factors in acute coronary syndrome have shown success, indicating that this approach is supported by prior research.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Diagnosed as acute coronary syndrome and needed to undergo percutaneous coronary intervention. * \>18 years old. Exclusion Criteria: * With malignant tumors, acute infectious diseases and advanced liver diseases. * Won't sign an inform consent.
Where this trial is running
Jinan, Shandong
- Jinan Central Hospital — Jinan, Shandong, China (Recruiting)
Study contacts
- Principal investigator: Guohao Su, doctor — Jinan Central Hospital
- Study coordinator: Guohai Su, doctor
- Email: huangrong9277@163.com
- Phone: +86-18854125717
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.