Clinical Trials Directory

Trials / Completed

CompletedNCT01398631

A Comparison of the TIMI, GRACE and HEART Scores

A Prospective Comparison of the TIMI, GRACE and HEART Scores for Predicting Cardiovascular Events in Chest Pain Patients in the Emergency Room

Status
Completed
Phase
Study type
Observational
Enrollment
2,440 (actual)
Sponsor
R&D Cardiologie · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

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.

Detailed 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.

Conditions

Timeline

Start date
2009-06-01
Primary completion
2010-12-01
Completion
2011-07-01
First posted
2011-07-20
Last updated
2016-02-17

Locations

10 sites across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT01398631. Inclusion in this directory is not an endorsement.