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Clinical Trials/NCT00284323
NCT00284323
Unknown
Phase 2

Beneficial Effect of Intracoronary Adenosine on Microvascular and Myocardial Salvage in Patients With Acute Myocardial Infarction (SALVAGE)

University Hospital, Gasthuisberg1 site in 1 country100 target enrollmentJanuary 2006

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Acute ST Elevation Myocardial Infarction
Sponsor
University Hospital, Gasthuisberg
Enrollment
100
Locations
1
Primary Endpoint
Beneficial Effect of Intracoronary Adenosine on Microvascular and Myocardial Salvage in Patients With Acute Myocardial Infarction
Last Updated
20 years ago

Overview

Brief Summary

Investigate the effect of selective intracoronary administration of adenosine on myocardial salvage and microvascular integrity in the setting of acute myocardial infarction.

Detailed Description

Prospective, single center, randomized clinical study. Study design is random patient assignment to selective intracoronary administration of adenosine or control immediately before restoration of coronary artery patency in patients presenting with an acute ST segment-elevation myocardial infarction (STEMI). Randomisation will be stratified for the duration of symptoms (\< 4 hours vs \> 4 hours).

Registry
clinicaltrials.gov
Start Date
January 2006
End Date
TBD
Last Updated
20 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University Hospital, Gasthuisberg

Eligibility Criteria

Inclusion Criteria

  • Myocardial infarction of less than 12 hours duration with symptoms lasting at least 20 minutes.
  • ECG-criteria: ST-segment elevation of \> 0.1 mV in 2 or more limb leads or \> 0.2 mV in 2 or more contiguous precordial leads or presumed new left bundle branch block.
  • Written informed consent prior to inclusion in the study. If this is not possible, verbal informed consent from the patient or written assent of a legally acceptable representative should be obtained, to be followed by written informed consent by the patient at the earliest subsequent opportunity.
  • Adequate vascular access seems possible (femoral pulsation palpable).

Exclusion Criteria

  • Contra-indication to heparin, LMWH, clopidogrel.
  • Anticipated difficulty with vascular access.
  • Cardiogenic shock.
  • Inability to give informed consent (or assent).
  • High grade atrioventricular block; severe asthma; treatment with theophylline, glibenclamide (Diamicron) or dipyridamole.
  • Prior CABG.
  • Participation in an investigational drug or device study within the past 30 days.

Outcomes

Primary Outcomes

Beneficial Effect of Intracoronary Adenosine on Microvascular and Myocardial Salvage in Patients With Acute Myocardial Infarction

By means of:

1. MR imaging

- at day 2-3: Rest perfusion, MVO, late enhancement and function

- at 4 months: Rest perfusion, late enhancement and function

2. Tissue Doppler Imaging

At 16-36 hours: Resolution of edema/wall thickness increase Function

At 4 months

3 Quantitative Coronary Angiography

TIMI flow grade, TIMI frame count on angiography of the IRA and myocardial blush grade before and at completion of the primary PCI procedure will be performed.

4 Electrocardiographic Analysis

- ST segment resolution will be assessed from the 12-lead ECG on admission and the ECG on admission on C.C.U. after the PCI-procedure. This will be examined for summed ST deviation and for ST deviation in the single lead with maximal ST-deviation on

Finally, the last ECG before hospital discharge and an ECG at 4 months will be studied for the evolution of Q-waves and T-waves.

- 24 hour continuous ST-segment recording in the single lead with maximal ST-deviation on admission with calculation of the area under the curve.

5 Echocardiographic evaluation of left ventricular function

At 16-36 hours

After 4 months

6 Cardiac markers

Blood samples for determination of the MB fraction of creatinekinase and of troponin I are to be taken:

On admission

Before and after PCI, through the sheath

At 90 minutes after PCI

At 8 hours after PCI

At 16 hours after PCI

At 24 hours after PCI

7 Clinical follow-up

Occurrence of MACE (death, new Q-wave or non Q-wave MI or target vessel revascularisation) and the presence of clinical signs of heart failure will be recorded

At hospital discharge

At 30 days

At 6 months

Study Sites (1)

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