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Completed

NCT Number: NCT01580566

Renal Acute MI Study

The purpose of this study is to determine if a sizable myocardial infarction (heart attack) results in negative changes to renal structure and function (i.e. has a negative impact on the kidneys).

To determine if the renal response to a myocardial infarction is a predictor of the patients future health.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Alfred Hospital

Melbourne, Victoria, 3004, Australia

About this study

Chronic heart and kidney disease are increasingly common in Western society. Both conditions are associated with frequent hospitalisation and increased mortality. Furthermore, there are mechanistic reasons why one condition may beget the other; the so-called "cardiorenal syndrome". The investigators therefore wish to determine if a sizable myocardial infarction (heart attack) results in negative changes to renal structure and function (i.e. has a negative impact on the kidneys). The investigators also wish to determine if the renal response to a myocardial infarction is a predictor of the patients future health. To do this the investigators will measure markers of kidney function at the time of the heart attach, at discharge, 1 month, 6 months and 12 months and correlate this with the patients clinical condition.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Age > 18 years

Have provided written informed consent

Group 1:

  • Non-Q wave MI patients
  • normal cardiac and renal function
  • No use of contrast
  • eGFR > 60ml/min

Group 2:

  • Patients undergoing coronary angiography +/- PCI for stable CAD or non-Q wave MI
  • normal cardiac and renal function
  • eGFR > 60ml/min

Group 3:

  • Acute STEMI Full thickness infarct (STEMI)
  • eGFR ≥ 60ml/min

Group 4:

  • Acute STEMI Full thickness infarct (STEMI)
  • eGFR < 60ml/min

Exclusion criteria

  • Unable or unwilling to comply with the study protocol
  • Underlying medical condition which, in the opinion of the investigator, will effect the safely or efficacy of the study

Treatment and study plan

Primary outcomes

  1. changes in renal function and structure

    Time frame: Baseline, discharge, 1 month, 6 months and 12 months

Secondary outcomes

  1. renal response to myocardial infarction

    Time frame: baseline, discharge, 1 month, 6 months and 12 months

Sponsors and collaborators

Lead sponsor

Monash University

Other

Registry information

Official study title

Renal Structural, Functional and Cytokine Responses to Acute Myocardial Injury in Man

Important dates

Study start
2012
Primary completion
2012
Study completion
2018
First posted
Apr 19, 2012
Registry last updated
Apr 3, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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