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Predictive Value of Risk Scores in Acute Coronary Syndrome

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT03549481
Recruitment Status : Recruiting
First Posted : June 8, 2018
Last Update Posted : August 23, 2018
Information provided by (Responsible Party):
shaimaa Mostafa, Benha University

Brief Summary:
role of different risk scores in acute coronary syndrome to predict left ventricular remodeling

Condition or disease
Acute Coronary Syndrome Left Ventricle Remodeling Risk Scores

Detailed Description:

patients with acute coronary syndrome (STEMI, NSTEMI, UA) will be included and different risk scores will be calculated for each patient.

after that in-hospital and short-term outcome beside left ventricular systolic and diastolic functions (at admission and 3m later) will be assessed to be correlated with different risk scores to determine which score system was able to predict left ventricular remodeling and what was the cut off value, sensitivity, and specificity of the score

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Study Type : Observational
Estimated Enrollment : 200 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Role of TIMI, PURSUIT and GRACE Risk Scores in Predicting LV Remodeling in Patients With Acute Coronary Syndrome
Actual Study Start Date : July 9, 2018
Estimated Primary Completion Date : January 2019
Estimated Study Completion Date : January 2019

Primary Outcome Measures :
  1. left ventricular remodeling [ Time Frame: 3 months ]
    end diastolic volume, end systolic volume, ejection fraction

  2. in hospital and short term outcme [ Time Frame: 3 months ]
    re-infarction, death, arrhythmia

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 80 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
adult patients of both gender with acute coronary syndrome

Inclusion Criteria:

  • patients with acute coronary syndrome

Exclusion Criteria:

  • previous acute coronary syndrome previous PCI or CABG chronic renal disease decompensated liver disease patient refusal to participate patients dropped during follow up

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 identifier (NCT number): NCT03549481

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Contact: shaimaa A Mostafa, MD 01229122843 ext 0020

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shaimaa Mostafa Recruiting
Cairo, Egypt
Contact: shaimaa A mostafa, MD         
Sponsors and Collaborators
shaimaa Mostafa

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Responsible Party: shaimaa Mostafa, assistant professor of cardiovascular medicicne, Benha University Identifier: NCT03549481     History of Changes
Other Study ID Numbers: 3 SH research
First Posted: June 8, 2018    Key Record Dates
Last Update Posted: August 23, 2018
Last Verified: August 2018

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Keywords provided by shaimaa Mostafa, Benha University:
risk score
acute coronary syndrome
left ventricular remodelng

Additional relevant MeSH terms:
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Acute Coronary Syndrome
Ventricular Remodeling
Pathologic Processes
Myocardial Ischemia
Heart Diseases
Cardiovascular Diseases
Vascular Diseases
Pathological Conditions, Anatomical