Actively Recruiting

Age: 18Years - 75Years
All Genders
ID06542653

Effect of Percutaneous Coronary Intervention on Clinical Outcomes in Patients with Chronic Coronary Artery Occlusion

Led by The First Affiliated Hospital with Nanjing Medical University · Updated on 2024-12-27

258

Participants Needed

1

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to assess whether successful percutaneous coronary intervention (PCI) can improve long-term outcomes compared to optimal medical therapy (OMT) in patients with coronary chronic total occlusions (CTOs). CTOs are linked to higher risks of adverse heart and brain events, so the study focuses on evaluating these risks and overall survival in affected patients. Participants included those treated at a hospital between 2011 and 2017, with the goal to understand if PCI offers better clinical prognosis than medication alone. The study compares two groups of CTO patients: those who underwent successful PCI and those treated with optimal medical therapy, which includes medications such as aspirin, ACE inhibitors or ARBs, beta blockers, and statins. Patients who had previously undergone coronary artery bypass grafting were excluded. The treatments were administered based on symptoms, viability of heart tissue, or evidence of ischemia in the area served by the blocked artery. Participants are monitored for major adverse cardiac and cerebrovascular events (MACCE), including cardiac death, recurrent heart attacks, unplanned revascularizations, and strokes, over a long period from January 2011 to December 2023. Secondary outcomes include all-cause death. The study collects data on these events to compare the effectiveness and safety of PCI versus medical therapy in improving the prognosis for patients with chronic coronary artery occlusions.

CONDITIONS

Official Title

Effect of PCI on Clinical Prognosis of Chronic Coronary Artery Occlusion

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with at least one coronary chronic total occlusion lesion treated at the hospital between January 2011 and December 2017
Not Eligible

You will not qualify if you...

  • Patients with ST-segment elevation myocardial infarction (STEMI)
  • History of coronary artery bypass grafting (CABG)
  • Cardiogenic shock
  • Malignant tumor

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The First Affiliated Hospital with Nanjing Medical University

Nanjing, Jiangsu, China, 210009

Actively Recruiting

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Research Team

M

Mei Wang

L

Lei Jiang

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

Frequently Asked Questions

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Effect of Percutaneous Coronary Intervention on Clinical Outcomes in Patients with Chronic Coronary Artery Occlusion | DecenTrialz