Efficacy of Implantable Defibrillator Therapy After a Myocardial Infarction
Status: | Active, not recruiting |
---|---|
Conditions: | Cardiology |
Therapuetic Areas: | Cardiology / Vascular Diseases |
Healthy: | No |
Age Range: | 18 - 80 |
Updated: | 6/9/2016 |
Start Date: | March 2011 |
End Date: | December 2021 |
Risk Estimation Following Infarction Noninvasive Evaluation - ICD Efficacy
This study will assess whether an implantable defibrillator will increase the likelihood of
survival in patients who have had a heart attack in the prior 5 years, have abnormal test
results from a 24 hour heart monitor, and who have low normal heart function.
survival in patients who have had a heart attack in the prior 5 years, have abnormal test
results from a 24 hour heart monitor, and who have low normal heart function.
The REFINE ICD trial will assess whether prophylactic ICD therapy, guided by non-invasive
risk assessment tools, reduces mortality in MI survivors with better-preserved LV function.
risk assessment tools, reduces mortality in MI survivors with better-preserved LV function.
Site investigators are responsible for screening. Subjects must meet all inclusion
criteria. Subjects with any exclusion criteria will be excluded.
Initial inclusion criteria (eligibility for Holter screening).
- 18 - 80 years old at time of consent
- History of MI > / = 2 and < / = 60 months prior to screening based on
ESC/ACCF/AHA/WHF criteria (both STEMI and NSTEMI subjects are eligible)
- Appropriate post-MI management including revascularization where indicated
- No contra-indication for transvenous ICD placement (e.g., mechanical tricuspid valve,
known vascular access problems, active sepsis, etc.)
- LVEF 36% - 50% measured 2 to 60 months after a confirmed MI, > / = 3 months after
coronary angioplasty or coronary bypass surgery and < / = 6 months of the screening
visit
- Proven, necessary or appropriate medications (e.g. beta-blocker, ACE inhibitor / ARB,
statin, and anti-platelet)
- In normal sinus rhythm (ECG documented) within the two weeks prior to the screening
Holter
- Written informed consent
- Able and willing to complete the screening Holter, including the six-minute hall walk
Additional inclusion criterion (eligibility for randomization).
• Abnormal HRT & TWA (core lab interpretation) on Holter performed 2 to 60 months after
the index MI and the specified time after coronary revascularization
Exclusion criteria (randomization or registry).
- Use of antiarrhythmic drugs
- Clinical indication for permanent pacemaker or a cardiac resynchronization device
- Clinical indication for an ICD or cardiac resynchronization ICD
- Prior implantation of a pacemaker, ICD, or Cardiac Resynchronization device
- Any condition, in the investigator's judgment, that would limit life expectancy to <
12 months
- Chronic renal failure (hemodialysis or peritoneal dialysis)
- Active ischemia that is amenable to revascularization if not previously
revascularized
- Participation in another trial that may interfere with the REFINE ICD results.
- Pregnancy
- Inability to comply with the follow-up schedule
We found this trial at
31
sites
University of Virginia The University of Virginia is distinctive among institutions of higher education. Founded...
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Cleveland Clinic Cleveland Clinic is committed to principles as presented in the United Nations Global...
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1211 Medical Center Dr
Nashville, Tennessee 37232
Nashville, Tennessee 37232
(615) 322-5000
Vanderbilt Univ Med Ctr Vanderbilt University Medical Center (VUMC) is a comprehensive healthcare facility dedicated...
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Ohio State University The Ohio State University’s main Columbus campus is one of America’s largest...
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The Valley Hospital The Valley Hospital is a fully accredited, acute care, not-for-profit hospital serving...
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