跳至主要内容
临床试验/NCT07145138
NCT07145138招募中不适用

University of Illinois Chicago (UIC) Multi-Ethnic Dilated Cardiomyopathy (DCM) Registry

University of Illinois at Chicago1 个研究点 分布在 1 个国家目标入组 1,500 人开始时间: 2024年7月11日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
1,500
试验地点
1
主要终点
Likely Pathogenic/Pathogenic Variants

研究概览

简要总结

Dilated cardiomyopathy (DCM), a condition where the heart loses its ability to pump blood throughout the body, is a common cause of death in the United States (US). It affects minorities more frequently and appears to causes greater harm than Whites. However, almost all research related to DCM has been performed in Whites, where up to half of cases run in the family. Several genes have been identified that cause the disease, but we are unsure if these same genes are also responsible for DCM in African Americans or Hispanic/Latino patients. The impact of various medical, social, and financial stressors on the severity of the disease in ethnic minorities also remains unclear. The investigators believe that certain genes are more common in different racial and ethnic groups and the greater medical, social, and financial burden faced by minorities in the US leads to more harm from DCM in these groups. The overall goal of the project is to test whether ethnic minority patients carrying genes that cause DCM experience more adverse effects in part because of various medical, social, and financial burdens. The investigators will first establish the UIC Multi-ethnic DCM Biorepository to look for how often certain genes are found across different race-ethnicity and then ask the question if these genes impact the severity of DCM. Finally, the investigators will study how a person's environment can alter the course of their disease. Through this, the investigators hope and strive to ensure equal and adequate heart care for individuals regardless of their race-ethnicity.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Must be at least 18 years of age and be admitted to or seen at a UIH site.
  • Subjects must be willing and able to give written, informed consent

排除标准

  • Adults who are unable to provide consent
  • Women who are pregnant at the baseline visit,
  • Prisoners
  • Individuals who are not yet adults (infants, children, teenagers).

结局指标

主要结局

Likely Pathogenic/Pathogenic Variants

时间窗: Baseline

Utilizing genomic sequencing, the investigators will obtain blood samples at baseline for study participants and identify utilizing genomic sequencing the prevalence of likely pathogenic/pathogenic (LP/P) variants in dilated cardiomyopathy patients across race-ethnicity.

次要结局

  • Severity of Disease Symptoms: Minnesota Living with Heart Failure Questionnaire (MLHFQ) Score(Participants with heart failure or who develop heart failure will complete the digital MLHFQ assessments at 12 months, 24 months, and 60 months after initial enrollment or new heart failure diagnosis.)

研究者

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

David Tofovic

Assistant Professor

University of Illinois at Chicago

研究点 (1)

Loading locations...

相似试验