Actively Recruiting

Age: 18Years - 85Years
All Genders
ID05719545

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

Age: 18Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with acute coronary syndrome and scheduled to undergo percutaneous coronary intervention
  • Aged over 18 years
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Up to 1 week

Participants undergo percutaneous coronary intervention and related diagnostic assessments.

1 visit (in-person)

Long-term Monitoring

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

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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

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