NL-OMON41965已完成不适用
HCMR - Novel Predictors of Outcome in Hypertrophic Cardiomyopathy. - HCMR (2222/0003)
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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