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临床试验/NCT04014946
NCT04014946已完成不适用

Prospective Assessment of Risk Factors for Appropriate ICD Intervention in Patients With Ischemic Cardiomyopathy

Biotronik SE & Co. KG0 个研究点目标入组 200 人开始时间: 2012年7月24日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
200
主要终点
Relative Infarct Transmurality

研究概览

简要总结

Design: PARCADIA is a prospective non-randomized non-interventional multi-center clinical investigation in Europe. Patients with depressed LV (left ventricular) function assessed on local standards, of ischemic origin and on chronic optimal medical therapy will be selected according to inclusion and exclusion criteria, implanted with an ICD after executing baseline investigations and prospectively followed up for minimal 24 months and until the termination of the clinical investigation.

General objective: analysis of baseline risk factors to identify predictors for appropriate ICD intervention in patients with ischemic cardiomyopathy receiving an ICD for primary prevention (MADIT II population).

Hypothesis: The primary alternative hypothesis states that the mean relative infarct transmurality (RIT) is different in patients with (RITshock or ATP (Anti Tachy Pacing)) and without (RITno shock or ATP )appropriate ICD intervention, i.e. shock or ATP.

  • Null hypothesis (H0): RITshock or ATP = RITno shock or ATP
  • Alternative hypothesis (Ha): RITshock or ATP ≠ RITno shock or ATP

Sample size: 200 patients.

Follow-up: Enrolment visit, pre implant screening, ICD implantation, pre-hospital discharge visit, and follow-up (FUP) visits at 2, 6, 12, 18, 24 months including home monitoring. Additional routine FUP every 6 months until study termination after last enrolled patient has completed 2 years FUP.

详细描述

Rationale: Implantation of an ICD as primary prevention therapy is indicated according to the current guidelines based on the low LVEF (Left Ventricular Ejection Fraction) as it was shown to significantly reduce mortality. Although of proven efficacy, ICD therapy is associated with survival benefit in only a small fraction of patients. It is estimated that 18 patients would have to receive an ICD to save one life, resulting in a huge burden on national health systems. Moreover, only about one quarter of all guideline eligible primary prevention ICD patients receive appropriate shocks. The above considerations support the need for an effective risk-stratification method to identify patients that benefit most (or least) from this therapy. Evaluation of ventricular anatomy and function by imaging techniques has become more important since this provides information on the substrate (myocardial scar) and trigger of life-threatening ventricular arrhythmias. Besides accurate estimation of left and right ventricular volumes and functions, Late Gadolinium Enhanced Cardiac Magnetic Resonance (LGE-CMR) imaging has a very high sensitivity to detect myocardial scar. Quantification of scar characteristics by cardiac MRI might be useful for the prediction of future arrhythmic events in patients with ischemic cardiomyopathy. However evidence is conflicting and published papers are hampered by limited patient numbers and can only be regarded in the light of generating hypothesis. The PARCADIA clinical investigation will explore the potential of cardiac MRI as a predictor for appropriate ICD intervention in a multicenter setting.

PARCADIA is a prospective non-randomized non-interventional multi-center clinical investigation in Europe. Patients with depressed LV (Left Ventricular) function assessed on local standards, of ischemic (at least 40 days post-MI (myocardial infarction) or 3 months post revascularization) origin and on chronic optimal medical therapy will be selected according to inclusion and exclusion criteria, implanted with an ICD after executing baseline investigations and prospectively followed up for minimal 24 months and until the termination of the clinical investigation

General objective: analysis of baseline risk factors to identify predictors for appropriate ICD intervention in patients with ischemic cardiomyopathy receiving an ICD for primary prevention (MADIT II population).

The primary objective of the clinical investigation is to determine whether there is a relationship between appropriate ICD intervention (shock or ATP) and the Relative Infarct Transmurality (RIT) obtained from Late Gadolinium Enhanced Cardiac Magnetic Resonance (LGE-CMR) imaging in patients with ischemic cardiomyopathy, receiving an ICD for primary prevention.

Methodology: Screening: (within 6 months before enrolment) patients with LV depressed function due to Ischemic Cardiomyopathy with an indication for primary prevention ICD implantation according to ESC (European Society of Cardiology) guidelines or local standards will be screened within 6 months before enrolment.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient with ischemic cardiomyopathy indicated for a de novo ICD implantation for primary prevention, according to ESC guidelines or local standards (MADIT II population)
  • Written informed consent / willingness and ability to comply with the protocol

排除标准

  • Contraindication for MRI
  • Severe renal dysfunction (stage 4 or 5) resulting in contra-indication for the admission of gadolinium during MRI (See Appendix A for more details)
  • Indication for secondary prevention ICD implantation
  • Class I indication for cardiac resynchronization therapy
  • Heart failure with New York Heart Association functional class IV
  • LV ejection fraction >40%
  • Age <18 years and >85 years
  • Women that are pregnant, lactating or planning to become pregnant
  • Participating in any other clinical trial with active intervention(s) during the course of this study
  • Life expectancy less than 1 year

结局指标

主要结局

Relative Infarct Transmurality

时间窗: Measured during Late gadolinium enhancement cardiovascular magnetic resonance (LGE-CMR) imaging within 3 months after inclusion and before ICD implantation

Percentage Relative Infarct Transmurality (RIT = transmural infarct mass / total infarct mass) obtained from LGE-CMR

appropriate ICD intervention (shock or ATP)

时间窗: Until the 24 month follow-up

assessment whether patient had appropriate ICD intervention (shock or ATP) or not during 24 months follow-up. ICD interventions will be labeled appropriate or non-appropriate by an independent endpoint committee.

次要结局

  • rhythm(baseline)
  • LV mass(Baseline)
  • total infarct mass(Baseline)
  • spontaneous episodes of atrial and ventricular arrhythmias(baseline)
  • heart rate variability (SDNN: Standard deviation of consecutive normal-to-normal intervals)(baseline)
  • QRS width(baseline)
  • serum sodium and potassium(baseline)
  • HR(baseline)
  • albumin(baseline)
  • incidence of hypercholesterolemia(baseline)
  • LV function (EF)(Baseline)
  • transmural infarct mass(Baseline)
  • NT-proBNP (N-terminal pro-hormone Brain Natriuretic Peptide)(baseline)
  • hsTNT/I (high sensitive Troponin-T/I)(baseline)
  • aldosterone(baseline)
  • incidence of hypertension(baseline)
  • mean Heart Rate (HR)(Baseline)
  • Day and night HR(baseline)
  • HbA1c (Hemoglobin A1c)(baseline)
  • PVC/hr: Premature ventricular contraction per hour(baseline)
  • uric acid(baseline)
  • incidence of diabetes(baseline)
  • serum creatinine(baseline)

研究者

申办方类型
Industry
责任方
Sponsor

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