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临床试验/NL-OMON41965
NL-OMON41965已完成不适用

HCMR - Novel Predictors of Outcome in Hypertrophic Cardiomyopathy. - HCMR (2222/0003)

niversity of Oxford0 个研究点目标入组 140 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
140

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • Male or Female, aged 18-65
  • Established diagnosis of HCM defined as unexplained LVH defined as any segment >= 15mm thick
  • Signed informed consent
  • Able (in the investigator's opinion) and willing to comply with all study requirements

排除标准

  • Uncontrolled hypertension as judged by the investigator
  • Uncontrolled atrial fibrillation at time of enrollment
  • Angiographically documented >50% coronary stenosis
  • Prior septal myectomy or alcohol septal ablation
  • Prior myocardial infarction
  • Incessant ventricular arrhythmias
  • Diabetes with end organ damage
  • Stage IV/V chronic kidney disease (eGFR <30ml/min)
  • Inability to tolerate MRI scanning (severe claustrophobia, inability to lie flat)
  • Contraindications to CMR imaging (implantable devices or other metal implants, cranial aneurysm clips, metallic ocular foreign bodies, hypersensitivity to gadolinium)
  • Female participant who is pregnant or lactating
  • Malignancy or other serious medical condition expected to limit lifespan <5 years
  • Any other significant disease or disorder which, in the opinion of the investigator, might influence the participant*s ability to participate in the study.
  • Involvement in other studies thought to compromise resulting study data or the health of the participant
  • Prior inclusion in the study of 5 members of the same immediate family.
  • Inability to give informed consent

研究者

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