Collects health data and samples from people with plasma cell disorders
Gathers health information and samples from adults with plasma cell disorders for future research.
Plain-language title generated from the registry record
Registry title: The Indiana Myeloma Registry
Key facts
- Where
- Indianapolis, United StatesSee the site
Where in United States
- Indiana University Simon Cancer CenterIndianapolis, United StatesTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Indiana University
- Trial code
- NCT03616483
- Record updated
- 29 October 2026
- Original description
This is a prospective, non-interventional, observational study. The purpose of this study is to collect data and bio-specimens that will support future researchRead full original descriptionShow less
Collection of Specimens and Clinical Data to Create A Bio-repository for the Multiple Myeloma Program: The Indiana Myeloma Registry
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
Inclusion: 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.
Exclusion: < 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.