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A Comparison of the TIMI, GRACE and HEART Scores

R

R&D Cardiologie

Status

Completed

Conditions

Acute Coronary Syndrome

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT01398631
Z-08.27

Details and patient eligibility

About

Various elements of patient history are checked and entered in the admission Case Recor Form (CRF). Three risk scores are calculated out of these elements, combined with physical examination, laboratory values and ECG-findings.

The primary aim is to assess the positive and negative predictive values for a cardiovascular event of the three risk scores for chest pain patients.

Secondary aim is to assess the sensitivity and specificity of various elements in the patient history for an acute coronary syndrome.

Full description

This is a prospective, observational study in patients admitted to the emergency room for chest pain. All patients are checked by the resident in charge immediately on admission, before any lab values are known, by means of an admission Case Report Form (CRF), consisting of classical elements of patient history, risk factors, medication and physical examination. This CRF is filled out immediately by the resident. No additional effort will be asked of the patients.

Patient data during a follow up of at least 6 weeks are gathered from hospital charts.

The predictive value of the three scoring systems: HEART (History, ECG, Age, Risk factors, Troponin), TIMI (Thrombolysis in Myocardial Infarction) and GRACE (Global Registry of Acute Coronary Events) for both the discharge diagnosis and the occurrence of Major Adverse Cardiovascular Events (MACE) is calculated.

The primary hypothesis of the study is that the HEART score is a significantly better predictor than the TIMI and/or GRACE score for cardiovascular events during a six week period following admission to the emergency room.

Enrollment

2,440 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • any patient visiting the cardiology emergency room due to chest pain

Exclusion criteria

  • chest pain clearly due to rhythm disturbances or acute heart failure
  • concomitant non cardiac disease with expected fatal outcome within 1 year

Trial design

2,440 participants in 1 patient group

Study Group
Description:
All included patients presented with chest pain at the emergency room within the inclusion period.

Trial contacts and locations

10

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Data sourced from clinicaltrials.gov

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