Menu
Not yet recruiting NCT06286215

Registry of Patients With Plasma Cell Disorders

Observational Plasma Cell Disorders

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Plasma Cell Disorders. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The goal of this observational study is to register patients with plasma cell disorders. The main questions it aims to answer are: * The incidence of plasma cell disorders both before and after malignancy * Time to progression of monoclonal gammopathy of undetermined significant (MGUS) or smoldering multiple myeloma (SMM) to light chain amyloidosis or multiple myeloma (MM) * Progression free survival (PFS) * overall survival * factors influencing overall survival, progression-free survival, and time to progression * Symptoms and signs of the disease during the diagnosis and relapse phases, including the causes of mortality in plasma cell disorder patients. * genetic characteristics of plasma cell disorder * cost-effectiveness of treatment in Thailand Participants will be collected the data of baseline diagnosis, treatment, treatment results of all admission and follow-up visits from hospital medical record.

Primary outcome measures

  • register the plasma cell disorder patients [Time frame: 10 years]
Secondary outcome measures (8)
  • incidence of plasma cell disorders [Time frame: 10 years]
  • Time to progression [Time frame: 10 years]
  • Progression free survival [Time frame: 10 years]
  • overall survival [Time frame: 10 years]
  • influencing factors [Time frame: 10 years]
  • Symptoms and signs [Time frame: 10 years]
  • genetic characteristics [Time frame: 10 years]
  • cost-effectiveness [Time frame: 10 years]

Eligibility criteria

Inclusion criteria

  • Both existing and newly diagnosed patients with plasma cell disorders, including monoclonal gammopathy of undetermined significance, smoldering multiple myeloma, POEMS, light chain amyloidosis, solitary plasmacytoma, and multiple myeloma, according to the diagnostic criteria of the International Myeloma Working Group 2014
  • Aged 18 years and above

Exclusion criteria

  • insufficient data needed for analysis

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06286215 · 586/2564(IRB2)

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗