NCT03616483招募中不适用
Collection of Specimens and Clinical Data to Create A Bio-repository for the Multiple Myeloma Program: The Indiana Myeloma Registry
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 2,500
- 试验地点
- 1
- 主要终点
- Create a repository
研究概览
简要总结
This is a prospective, non-interventional, observational study. The purpose of this study is to collect data and bio-specimens that will support future research
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 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
- 否
入选标准
- •Male or female patients ≥ 18 years of age at the time of informed consent
- •Has been diagnosed with or is suspected to have one of the following:
- •Monoclonal Gammopathy of Undetermined Significance (MGUS)
- •Smoldering Multiple Myeloma
- •Multiple Myeloma
- •Bony or Soft Tissue Plasmacytoma
- •Primary Amyloidosis
排除标准
- •< 18 years of age
- •Have not been diagnosed with one of the following:
- •Monoclonal Gammopathy of Undetermined Significance (MGUS) b.Smoldering Multiple Myeloma c.Multiple Myeloma d.Bony or Soft Tissue Plasmacytoma e.Primary Amyloidosis
结局指标
主要结局
Create a repository
时间窗: 5 years
The primary objective of this study is to provide a mechanism to store comprehensive clinical, genomic, demographic, social, environmental and quality of life data from subjects with plasma cell dyscrasias
次要结局
- Data collection(5 years)
研究者
Attaya Suvannasankha
Clinical Professor of Clinical Medicine
Indiana University
研究点 (1)
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