Comparison of Two Treatment Strategies in Patients With an Acute Coronary Syndrome Without ST Elevation

Overview

The acute coronary syndrome (ACS) without ST elevation is a frequent pathology. The main evolutionary risk of these patients is the coronary thrombosis and its self complications. The platelets aggregation plays a major role in the physiopathology of the ACS. The therapeutic arsenal of the anti-thrombosis essentially resting on aspirin and heparin has been reinforced lately by the inhibitors of the glycoprotein anti GP IIb/IIIa. The profit of these products in the ACS with or without ST elevation, associated or not to coronarography, has clearly been demonstrated. This profit is more marked when patients are at high risk of complications. Thus, the use of an anti GP IIb/IIIa is recommended among patients at "high risk" for whom a coronarography is planned, in the last international recommendations of the European Cardiology Society (ESC), the American Heart Association and the American College of Chest Physician. Otherwise, some authors have proposed An early invasive strategy based on coronarography with discordant results. The ideal delay of realization of this coronarography is unknown. It varies according to the studies between 2.5 hours to 48 hours. Once again, patients at high risk seem to benefit the more of such a strategy if it is set precociously. Objective To compare an invasive strategy associating an early administration of tirofiban and a coronarography achieved in the 6 hours after the randomization to a conservative strategy in a population of high risk patients with ACS without ST elevation. Design Multicentric, prospective, randomized study.

Full Title of Study: “Treatment by Anti GP IIb/IIIa in the Setting of a Strategy of Early Coronarography to Patients With an Acute Coronary Syndrome Without ST Elevation”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Parallel Assignment
    • Primary Purpose: Treatment
    • Masking: None (Open Label)
  • Study Primary Completion Date: December 2010

Detailed Description

Patient's selection Patient of more than 18 years with a ACS defined by a thoracic pain of more than 20 minutes that occurred during the last 24 hours, anomalies on EKG and one of the following criteria : diabetes; recurrence of coronary pain; precocious pain post-myocardial infarction; falling of the ST segment of > 1 mm; transient elevation of the ST segment > 1 mm; elevation of the I troponin, T troponin or CPK MB; hemodynamic instability; ventricular arrhythmia; TIMI score > 5 Therapeutic modes All patients receive : aspirin, clopidogrel, enoxaparine. Trinitrin and analgesics are at the clinician's appreciation. Besides, either they receive an anti GP IIb/IIIa: tirofiban (Agrastat®) and are oriented in cardiology to have a coronarography in the six hours or they are oriented in cardiology to receive the classical treatment, guided by the investigations searching for signs of myocardial ischemia.

Interventions

  • Drug: TIROFIBAN
    • intravenous infusion
  • Procedure: CORONAROGRAPHY
    • standard procedure of coronarography

Arms, Groups and Cohorts

  • Experimental: Early Invasive strategy
    • Tirofiban and coronarography within 6 hours
  • Active Comparator: Delayed invasive strategy
    • Coronarography after 6 hours

Clinical Trial Outcome Measures

Primary Measures

  • Mortality, Myocardial Infarction and Revascularization in Emergency
    • Time Frame: d30

Secondary Measures

  • Therapeutic Failure (Well Defined) During the First 6 Hours. Clinical Evolution and Electrocardiography
    • Time Frame: until the exit from the hospital and at d30.
  • Coronarographic Criteria : TIMI Score at the Beginning and the End of the Procedure; Existence of an Intra-coronary Thrombus
    • Time Frame: d30
  • Troponin Peak. Left Ventricular Ejection Fraction Before Hospital Exit. Length of Stay in USIC and Hospital. Hemorrhagic Complications.
    • Time Frame: d30

Participating in This Clinical Trial

Inclusion Criteria

  • High risk ACS without ST elevation Exclusion Criteria:

  • Age <18 years – Pregnancy – Persistence of the ST elevation – Recent left branch block – Cardiac failure or cardiogenic shock (Kilip 3 or 4) – Treatment by anti-vitamin K – Contra-indication to the use of one of the following treatments: aspirin, clopidogrel, enoxaparine, anti GP IIb/IIIa (tirofiban)

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Hospital Avicenne
  • Provider of Information About this Clinical Study
    • Principal Investigator: FREDERIC LAPOSTOLLE, Frédéric Lapostolle – Hospital Avicenne
  • Overall Official(s)
    • FREDERIC LAPOSTOLLE, MD, Principal Investigator, SAMU 93 – AVICENNE HOSPITAL
    • FREDERIC ADNET, PHD, Study Director, SAMU 93 – AVICENNE HOSPITAL

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