ISRCTN35774505已完成未知
Follow-up care by a specialized genetic counsellor for patient relatives at risk for cardiomyopathies is cost-saving and well-appreciated: a randomised comparison
niversity Medical Center Groningen (Netherlands)0 个研究点目标入组 189 人开始时间: 2016年4月23日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 189
研究概览
简要总结
2017 results in https://www.ncbi.nlm.nih.gov/pubmed/27901040 (added 09/08/2019)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Aged > 16 years
- •2. Relative of patients with DCM/ HCM or mutation carriers
- •3. Participants must be either:
- •3.1. Carriers of mutations in the LMNA, DES or PLN genes, who are at a higher prior risk for malignant ventricular arrhythmias compared to other groups; or
- •3.2. Phenotype-negative relatives (over 16 years of age) of index patients with DCM or HCM with a proven pathogenic mutation and therefore at risk for developing DCM or HCM; or
- •3.3. Phenotype-negative relatives of index patients with potentially inherited DCM or HCM in whom no pathogenic mutation had been identified
排除标准
- •1. Any signs or symptoms of the disease
- •2. Presence of other heart diseases
- •3. A medical history with complex co-morbidity
研究者
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