跳至主要内容
临床试验/NCT02398786
NCT02398786招募中不适用

Myotonic Dystrophy Family Registry

Myotonic Dystrophy Foundation1 个研究点 分布在 1 个国家目标入组 3,500 人开始时间: 2013年2月最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
3,500
试验地点
1
主要终点
Patient reported outcomes

研究概览

简要总结

The Myotonic Dystrophy Family Registry (MDFR) is an online, patient-entered database that collects information on myotonic dystrophy (DM) to aid researchers in developing new, effective treatments and help identify participants for research studies and clinical trials.

详细描述

The Myotonic Dystrophy Family Registry (MDFR) is an online, patient-entered database that collects information on myotonic dystrophy (DM) such as disease symptoms and demographic information to aid researchers in developing new, effective treatments and help identify participants for research studies and clinical trials.

The Registry supports trials and studies, making it easier for researchers to explore data and identify possible trial and study participants. It is the first DM registry that gives community members the opportunity to explore anonymous Registry data, to see what the DM community looks like and what others with DM experience. It also provides information on the community of people living with DM, giving researchers and other medical professionals the opportunity to improve how they treat those affected with DM and learn more about how and why certain treatments work and don't work.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Diagnosed with congenital, juvenile-onset or adult onset DM1 or DM2 (confirmed by clinical exam or genetic test)

排除标准

  • Not diagnosed with DM, unaffected family members

结局指标

主要结局

Patient reported outcomes

时间窗: 36 months

Number of patients reporting specific symptoms and symptom severity, as well as impacts to quality of life and overall burden of disease in order to inform clinical trial development, understanding of disease for academic, industry and federal agency stakeholders and overall policy decisions. Results will be analyzed in comparison to other registry data and surveys to characterize this disease population cohort and to further define the population.

次要结局

未报告次要终点

研究者

发起方
Myotonic Dystrophy Foundation
申办方类型
Other
责任方
Sponsor

研究点 (1)

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