Actively Recruiting

Age: 18Years - 70Years
All Genders
NCT06586424

The Prognostic Value of Anion Gap in Predicting Major Adverse Cardiovascular Events Among Patients With ST-Segment Elevation Myocardial Infarction

Led by Universitas Diponegoro · Updated on 2024-09-19

80

Participants Needed

1

Research Sites

39 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to evaluate the prognostic value of the anion gap in predicting major adverse cardiovascular events among patients with ST-segment elevation myocardial infarction. Researchers will collect information based on hospital registry as secondary data of in patient who had diagnosed as ST-segment elevation myocardial infarction and underwent primary percutaneous coronary intervention. The data consist of demographic data, clinical presentation, laboratory, and angiography result were collected from hospital registry by reviewing medical record. Then, the data was analyzed by using IBM SPSS Statistics v26.

CONDITIONS

Official Title

The Prognostic Value of Anion Gap in Predicting Major Adverse Cardiovascular Events Among Patients With ST-Segment Elevation Myocardial Infarction

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults with 18 to 70 years old diagnosed with ST-segment elevation myocardial infarction who underwent primary percutaneous coronary intervention
Not Eligible

You will not qualify if you...

  • History of heart failure due to any causes
  • Cardiogenic shock before primary percutaneous coronary intervention
  • Any infection at the time of presentation
  • Pregnant woman
  • Other causes of high anion gap such as chronic kidney disease or metabolic acidosis

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

Dr. Kariadi Central General Hospital

Semarang, Central of Java, Indonesia

Actively Recruiting

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Research Team

L

Leo Deddy Pradipta

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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