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STEMI Versus NSTEMI: Clinical and Angiographic Differences

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ClinicalTrials.gov Identifier: NCT01636427
Recruitment Status : Completed
First Posted : July 10, 2012
Last Update Posted : July 18, 2012
Information provided by (Responsible Party):
Ferrara Liberato Aldo, Federico II University

Brief Summary:
The purpose of this study is to assess differences in the risk profile and in the coronary angiographic presentation between STEMI and NSTEMI. Moreover possible relationship between myocardial infarction presentation and renal function will be investigated.

Condition or disease
Acute Coronary Syndrome

Detailed Description:

Assessment of risk profile. Diabetes mellitus diagnosed when fasting blood glucose (FBG) was >= 126mg/dL or if patients were taking oral hypoglycaemic drugs or were on insulin treatment. Hypertension defined as blood pressure >= 140/90 mmHg or history of antihypertensive treatment. Hypercholesterolemia,adjudicated when cholesterol levels were >= 200 mg/dL or with patients on lipid lowering treatment. Hypertriglyceridemia adjudicated on fasting triglyceride levels>= 200 mg/dL or triglyceride-lowering therapy . Obesity, defined as BMI >= 30 kg/m2.

Patients with STEMI, who had not been previously treated with thrombolysis, and those who had been undergone to an unsuccessful thrombolysis, as well as patients with NSTEMI with a TIMI score> 3 who were immediately referred to the Cat Lab and whenever possible treated with PTCA and stenting of the culprit lesion. The other patients who were referred to Cat Lab within 48 hours from the beginning of chest pain, unless their general conditions did not strongly suggest to delay the procedure after 2 more days.

Study Type : Observational
Actual Enrollment : 200 participants
Observational Model: Case-Only
Time Perspective: Retrospective
Official Title: STEMI Versus NSTEMI: a Mono Versus a Multivessel Disease?
Study Start Date : January 2007
Primary Completion Date : May 2012
Study Completion Date : May 2012

Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Patients with acute myocardial infarction with or without ST segment elevation.

Inclusion Criteria:

  • Patients admitted in the coronary care unit (CCU) of the Department of Clinical and Experimental Medicine at the Federico 2nd University Hospital;
  • Patient with indication to angiographic study even if not immediately;
  • Patients referred to CCU with the diagnosis of acute myocardial infraction (AMI), type STEMI, or NSTEMI, based on pre-admission assessment of troponin I (TpI) and myocardial band creatin kinase (CK-MB;
  • Diagnosis of NSTEMI/STEMI performed according to standard criteria

Exclusion criteria:

  • Patients who could not undergo angiographic study

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01636427

CCU Dipartimento Assistenziale di Clinica Medica
Naples, Italy, 80131
Sponsors and Collaborators
Federico II University
Study Director: Giovanni de Simone, MD Federico 2nd University of Naples

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Ferrara Liberato Aldo, Associate Professor of Medicine, Federico II University
ClinicalTrials.gov Identifier: NCT01636427     History of Changes
Other Study ID Numbers: 001
First Posted: July 10, 2012    Key Record Dates
Last Update Posted: July 18, 2012
Last Verified: July 2012

Keywords provided by Ferrara Liberato Aldo, Federico II University:
myocardial infarction
coronary angiography

Additional relevant MeSH terms:
Acute Coronary Syndrome
Myocardial Ischemia
Heart Diseases
Cardiovascular Diseases
Vascular Diseases