ComParative Diagnostic Study Between Multislice Computed Tomography (MSCT) and Stress Echography in Coronarin Patients. (PEPSI)
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Purpose
The aim of this study is to define the best prognostic strategy for patients presenting suspected acute CORONARY syndrome, between MSCT and stress echocardiography.
| Condition | Intervention |
|---|---|
|
Chest Pain |
Procedure: MSCT and stress echocardiography |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Diagnostic |
| Official Title: | ComParative Diagnostic Study Between MSCT and Stress Echography in Patients Presenting With Suspected Acute Coronary Syndrome Without ST Segment Elevation. |
- Relative diagnostic accuracy of stress echography and MSCT at presentation of patients with acute chest pain and suspected acute coronary syndrome [ Time Frame: 2 days ] [ Designated as safety issue: No ]
- proportion of AE in patients tested negative at both examinations: death, myocardial infraction, percutaneous coronary intervention, coronary artery bypass graft or readmission for chest pain with coronarography visualizing a stenosis greater than 50%. [ Time Frame: 6 months ] [ Designated as safety issue: No ]
- proportions of false positives, the reference method being coronarography. [ Time Frame: 2 days ] [ Designated as safety issue: No ]
- proportions of non interpretable or non contributory examinations [ Time Frame: 2 days ] [ Designated as safety issue: No ]
| Enrollment: | 217 |
| Study Start Date: | September 2008 |
| Study Completion Date: | March 2011 |
| Primary Completion Date: | September 2010 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: whole population who receive both tests
this arm includes the whole study population who will receive both tests: MSCT and stress echocardiography
|
Procedure: MSCT and stress echocardiography
tests MSCT and stress echocardiography
Other Name: tests MSCT and stress echocardiography
|
Detailed Description:
Patients presenting with a suspected acute CORONARY syndrome is based on the interrogation, the realization of an electrocardiogram (ECG) and 2 dosages of the cardiac troponin at some hours of interval. However, the ECG and the troponin are frequently normal and this does not absolutely eliminate the diagnosis. In that case, it is at present recommended to practise an effort ECG or a stress imaging, such as echocardiography. Several studies estimated the diagnostic exactness of stress echography for patients presenting a recent chest pain without modification of the ECG nor a rise of the troponin with a sensibility from 71 to 86% and a specificity from 91 to 98%. Recently, several teams estimated the interest of multislice computed tomography (MSCT) in the same population. The MSCT sensibility reported by 2 teams is promising because was found between 91 and 100%. On the other hand, the specificity was appreciably less good : between 76 and 82%. The negative predictive value to MSCT was excellent : between 97 and 100%.The aim of this work is to compare the diagnostic exactness between stress echography and MSCT for patients presenting with a suspected acute coronary syndrome without modification of the ECG nor rise of the troponin. It is about a prospective monocentric diagnostic study concerning 400 patients. The primary end point is the proportion report of true positives in MSCT with regard to stress echocardiography (the main diagnosis is the coronarography). The secondary end points include the proportion of false positives, the non interpretable or non contributory examination rate and especially the proportion of unwanted events in 6 months for the negative patients in both examinations according to a combined criteria including death, myocardial infraction (MI), percutaneous CORONARY intervention (PCI), coronary artery bypass graft (CABG) or readmission for chest pain with coronarography visualizing a stenosis greater than 50 %.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- chest pain < 24 hours
- normal ECG
- normal troponin I
Exclusion Criteria:
- ECG evolution
- troponin I evolution
- hemodynamic instability
- rhythmic instability
- allergy to iodized contrast products
- Creatinin > 150 micromol/L
- venous capital absence
- auricular fibrillation
Contacts and Locations| France | |
| Hospital european Georges pompidou | |
| Paris, France, 75015 | |
| Principal Investigator: | Eric DURAND, MD PH | Assistance Publique - Hôpitaux de Paris |
More Information
No publications provided
| Responsible Party: | Assistance Publique - Hôpitaux de Paris |
| ClinicalTrials.gov Identifier: | NCT00709670 History of Changes |
| Other Study ID Numbers: | P070607 |
| Study First Received: | July 2, 2008 |
| Last Updated: | February 13, 2013 |
| Health Authority: | France: Ministry of Health |
Keywords provided by Assistance Publique - Hôpitaux de Paris:
|
MSCT Echocardiography Coronarography Acute coronary syndrome without ST segment elevation |
normal ECG normal troponin Acute |
Additional relevant MeSH terms:
|
Chest Pain Acute Coronary Syndrome Pain Signs and Symptoms Myocardial Ischemia |
Heart Diseases Cardiovascular Diseases Angina Pectoris Vascular Diseases |
ClinicalTrials.gov processed this record on May 23, 2013