跳至主要内容
临床试验/NCT03398369
NCT03398369招募中不适用

Advanced Imaging and Inflammatory Markers to Define Mechanisms of Response to CRT

University of Virginia1 个研究点 分布在 1 个国家目标入组 180 人开始时间: 2018年1月5日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
180
试验地点
1
主要终点
Left ventricular end-systolic volume (LVESV) improvement

研究概览

简要总结

This is a mechanistic clinical trial with randomization to guidance for the CRT procedure using cardiac magnetic resonance (CMR) and computed tomography angiography (CTA) versus a standard procedure.

详细描述

At baseline, patients will have CMR, CTA, echocardiography, blood testing, and cardiopulmonary exercise testing. They will also complete a heart failure questionnaire. In patients randomized to CMR guidance for the CRT procedure, LV lead placement will be guided by the MRI information related to scar, activation and anatomy. Patients will have follow-up assessments at 6 and 12 months. There will also be clinical follow-up for survival free of appropriate ICD therapies over 3 years.

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
Single (Participant)

入排标准

年龄范围
20 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Chronic systolic HF
  • •LVEF 35% or less
  • •Guideline-based class I or II indication for CRT

排除标准

  • •Inability to provide informed consent
  • •Presence of metal embedded in the body due to prior accident or injury, as documented by skull films or other imaging
  • •Cerebral aneurysm clips
  • •Cochlear implants
  • •Other metallic implants known to be contraindications to CMR (does not include pacemakers and ICDs)
  • •Severe claustrophobia
  • •Acute kidney injury
  • •Acute renal failure or chronic kidney disease with GFR < 45 cc/min/1.73m2
  • •Liver transplant
  • •Gadolinium allergy
  • •>10% premature ventricular contraction (PVC) burden; and 13) estimated >10% atrial fibrillation (AF) burden based on available clinical data.

研究组 & 干预措施

Intervention

Experimental

CMR-Guided CRT

干预措施: CMR/CTA Guidance for CRT (Diagnostic Test)

Control

No Intervention

Standard CRT

结局指标

主要结局

Left ventricular end-systolic volume (LVESV) improvement

时间窗: One Year

Change in LVESV with cardiac resynchronization therapy (CRT)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kenneth Bilchick, MD

Associate Professor of Medicine

University of Virginia

研究点 (1)

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