Actively Recruiting

Age: 18Years +
All Genders
ID04988672

OPTIMISER Registry - A Prospective Cohort Study to Describe the Optimal Management and Outcomes of Patients Presenting With Acute Myocardial Infarction

Led by Luzerner Kantonsspital · Updated on 2023-10-06

4000

Participants Needed

1

Research Sites

208 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are collecting detailed data on patients who have had an acute myocardial infarction (AMI), commonly known as a heart attack, and received treatment with percutaneous coronary intervention (PCI). This observational study aims to assess procedural success, short- and long-term cardiovascular outcomes, and the performance of different devices and treatment strategies in managing AMI. The study also evaluates device-related complications, antithrombotic treatments, and economic factors related to interventional care for coronary artery disease (CAD). Participants who have experienced AMI, including both STEMI and NSTEMI types, and have undergone PCI or coronary artery bypass grafting (CABG) will have their clinical and procedural data collected both prospectively and retrospectively. Various devices such as balloons, stents, and scaffolds used during PCI will be studied for their effectiveness and safety. The study includes analysis of angiographic and optical coherence tomography (OCT) findings and investigates predictors of device failure and clinical outcomes over time. Participants will be monitored for major adverse cardiac and cerebrovascular events (MACCE), including new heart attacks, strokes, and cardiovascular deaths, with primary outcomes assessed at one year and extended follow-up up to ten years. Data will include hospitalizations, heart failure, arrhythmias, bleeding events, and procedural complications. Clinical outcome data, imaging results, and economic impacts will be recorded to enhance understanding of optimal AMI management and long-term patient prognosis.

CONDITIONS

Brief Title

OPTIMISER Registry - A Prospective Cohort Study to Describe the OPTIMal Management and Outcomes of PatIents PreSEnting With Acute MyocaRdial Infarction

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Newly diagnosed with acute myocardial infarction (STEMI or NSTEMI) or diagnosed within the last 5 years
  • Willing to sign informed consent or have a relative/proxy provide consent
  • Patients who have signed the General Consent
Not Eligible

You will not qualify if you...

  • Unwilling or unable to provide informed consent
  • Patients without acute coronary syndrome or acute myocardial infarction, such as those with Takotsubo cardiomyopathy or acute heart failure unrelated to AMI

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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)

Monitoring

Duration - Up to 10 years

Participants who have had an acute myocardial infarction are observed to assess procedural success, clinical outcomes, and complications over time.

Visits at 1, 2, 5, and 10 years

Trial Site Locations

Total: 1 location

1

Luzerner Heart Centre

Lucerne, Switzerland, 6000

Actively Recruiting

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Research Team

F

Florim Cuculi, M.D.

M

Matthias Bossard, M.D.

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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Published Research Related To This Trial

Trajectories of Cardiac Function Following Treatment With an Impella Device in Patients With Acute Anterior ST-Elevation Myocardial Infarction.

Gregorio Tersalvi, Adrian Attinger-Toller, Dhanya Kalathil...

https://pubmed.ncbi.nlm.nih.gov/36700188

Deferring stent optimization in stent thrombosis: A novel approach for STEMI management-Insights from a case series.

Giacomo Maria Cioffi, Mehdi Madanchi, Matthias Bossard...

https://pubmed.ncbi.nlm.nih.gov/33768799