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临床试验/NCT01324453
NCT01324453已完成1 期

Phase II Clinical Trial to Evaluate the Benefits of Postconditioning in STEMI

Minneapolis Heart Institute Foundation2 个研究点 分布在 1 个国家目标入组 103 人开始时间: 2011年3月最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
103
试验地点
2
主要终点
Infarct Size on Baseline Cardiac Magnetic Resonance Imaging (cMRI)

研究概览

简要总结

This study will evaluate change in heart muscle function from baseline to three months and twelve months in participants who present with a heart attack and a completely occluded coronary artery. These subjects will be randomized to receive standard Percutaneous transluminal coronary angioplasty (PTCA)/Stenting to open the artery or routine PTCA/Stenting plus post conditioning. Post conditioning commences immediately upon reperfusion using four cycles of thirty second inflations with a standard angioplasty balloon followed by a thirty seconds of reperfusion. The investigators hypothesize that Postconditioning reduces the size of the heart attack when utilized with successful primary Angioplasty/stent.

详细描述

Single center study involving 140 patients randomized to Post Conditioning + Percutaneous coronary intervention (PCI) versus routine PCI during their ST-Elevation Myocardial Infarction (STEMI, Heart Attack) presentation. The Post Conditioning protocol consists of performing four, 30-second PTCA (Angioplasty) balloon occlusions followed by 30-seconds of reperfusion over a total of 4 minutes. The first balloon inflation occurs immediately after an angioplasty guidewire is placed through the obstruction in the artery. Following this protocol the vessel is stented as part of the usual practice for treatment of STEMI. No other treatment differences will occur between the two groups and all patients will receive the usual post-STEMI care. Patients in both groups will receive a cardiac MRI 3-5 days following their STEMI for measurement of heart attack size and heart muscle function, among other measures. Patients will undergo collection of blood for creatine kinase (CK)-MB and troponin I every 8 hours for 24 hours following PCI. All patients will be followed by phone follow-up visits to review history and major adverse cardiac event (MACE) (death, recurrent STEMI, repeat revascularization, arrhythmias, implantable cardioverter-defibrillator (ICD) placement and hospitalization for congestive heart failure (CHF)). All patients will be required to take P2Y12 inhibitors and aspirin for the duration of the trial. All patients will be treated with angiotensin-converting enzyme inhibitor (ACE-I), beta blockers and statins.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age > 18 years old, < 80 years old
  • Able to give informed consent
  • Able to undergo cMRl (cardiac magnetic resonance imaging
  • ST-segment elevation infarction with 100% occlusion of a major epicardial vessel (> 2.5 mm)
  • No angiographic evidence of collateral flow distal to occluded artery
  • Ischemic duration between 1.0 and 6 hours
  • Thrombolysis in myocardial infarction (TIMI) 3 Flow following PCI

排除标准

  • Visible collateral blood flow to the distal vasculature of the occluded vessel
  • Previous Coronary Artery Bypass Graft surgery
  • Previous q-wave myocardial infarction in the same territory
  • Inability to give informed consent
  • Inability to undergo cMRl
  • Life expectancy less than one year
  • History of Non-compliance or alcohol or drug addiction
  • Patients with cardiogenic shock, cardiac arrest, hypothermia on presentation
  • Chronic dialysis or significant renal insufficiency (Creatinine Clearance < 35 mI/mm/i .73 m2)
  • TIMI Flow > 0 on presentation
  • Ischemic Time > 6 hours or < 1.0 hours
  • Presence of significant valvular heart disease (>mod Aortic Stenosis, >2+ Mitral Regurgitation)
  • Known Left Ventricular systolic dysfunction (Left Ventricular Ejection Fraction < 50% prior to STEMI)

研究组 & 干预措施

Post conditioning + PCI

Experimental

干预措施: Post Conditioning + Primary PCI (Procedure)

Standard PCI

Active Comparator

干预措施: Standard Primary PCI (Procedure)

结局指标

主要结局

Infarct Size on Baseline Cardiac Magnetic Resonance Imaging (cMRI)

时间窗: Day 3-5 post-PCI

Infarct size was quantified by delayed, contrast-enhanced MRI

Myocardial Salvage Index (MSI) on Baseline cMRI

时间窗: Day 3-5 post-PCI

The myocardial salvage index (MSI) was calculated using the formula: MSI = (AAR - Infarct size) / AAR X 100 % where quantitative estimation of myocardium at risk (AAR) was measured as the hyperintense region on T2- weighted imaging. Measurements were performed using the QMass software package (Medis mc, Raleigh NC) by a single investigator who was blinded to treatment. The endocardial and epicardial borders were manually identified and the regions of interest (edema or scar) were automated as 2 standard deviations above the mean density of the myocardium.

Micro Vascular Obstruction (MVO) on Baseline cMRI

时间窗: Day 3-5 post-PCI

High T1 imaging was utilized for the determination of the presence or absence of MVO.

次要结局

  • Global Left Ventricular Ejection Fraction(baseline)
  • Infarct Size by Peak Creatine Kinase (CK)(over first 72 hours post PCI)
  • Left Ventricular Remodeling (Left Ventricular End Systolic Volume - LVESV) as Measured by cMRl(baseline)
  • Infarct Size by Peak Troponin(over first 72 hour post PCI)
  • Left Ventricular Remodeling (Left Ventricular End Diastolic Volume - LVEDV) as Measured by cMRl(baseline)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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