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

Primary Purpose

CORONARY DISEASE

Status
Terminated
Phase
Phase 4
Locations
France
Study Type
Interventional
Intervention
TIROFIBAN
CORONAROGRAPHY
Sponsored by
Hospital Avicenne
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for CORONARY DISEASE focused on measuring CORONARY DISEASE

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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)

Sites / Locations

  • Samu 93 - Chu Avicenne

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Early Invasive strategy

Delayed invasive strategy

Arm Description

Tirofiban and coronarography within 6 hours

Coronarography after 6 hours

Outcomes

Primary Outcome Measures

Mortality, Myocardial Infarction and Revascularization in Emergency

Secondary Outcome Measures

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

Full Information

First Posted
March 7, 2007
Last Updated
February 9, 2015
Sponsor
Hospital Avicenne
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1. Study Identification

Unique Protocol Identification Number
NCT00445263
Brief Title
Comparison of Two Treatment Strategies in Patients With an Acute Coronary Syndrome Without ST Elevation
Acronym
SISCA
Official Title
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
Interventional

2. Study Status

Record Verification Date
February 2015
Overall Recruitment Status
Terminated
Why Stopped
Because of inclusion delay
Study Start Date
March 2007 (undefined)
Primary Completion Date
December 2010 (Actual)
Study Completion Date
July 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Avicenne

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
CORONARY DISEASE
Keywords
CORONARY DISEASE

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
170 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Early Invasive strategy
Arm Type
Experimental
Arm Description
Tirofiban and coronarography within 6 hours
Arm Title
Delayed invasive strategy
Arm Type
Active Comparator
Arm Description
Coronarography after 6 hours
Intervention Type
Drug
Intervention Name(s)
TIROFIBAN
Other Intervention Name(s)
IIb/IIIa GP inhibitor
Intervention Description
intravenous infusion
Intervention Type
Procedure
Intervention Name(s)
CORONAROGRAPHY
Other Intervention Name(s)
angiography
Intervention Description
standard procedure of coronarography
Primary Outcome Measure Information:
Title
Mortality, Myocardial Infarction and Revascularization in Emergency
Time Frame
d30
Secondary Outcome Measure Information:
Title
Therapeutic Failure (Well Defined) During the First 6 Hours. Clinical Evolution and Electrocardiography
Time Frame
until the exit from the hospital and at d30.
Title
Coronarographic Criteria : TIMI Score at the Beginning and the End of the Procedure; Existence of an Intra-coronary Thrombus
Time Frame
d30
Title
Troponin Peak. Left Ventricular Ejection Fraction Before Hospital Exit. Length of Stay in USIC and Hospital. Hemorrhagic Complications.
Time Frame
d30

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
FREDERIC LAPOSTOLLE, MD
Organizational Affiliation
SAMU 93 - AVICENNE HOSPITAL
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
FREDERIC ADNET, PHD
Organizational Affiliation
SAMU 93 - AVICENNE HOSPITAL
Official's Role
Study Director
Facility Information:
Facility Name
Samu 93 - Chu Avicenne
City
Bobigny
State/Province
Ile de France
ZIP/Postal Code
93000
Country
France

12. IPD Sharing Statement

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

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