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Registry of Patients With Plasma Cell Disorders

Registry of Patients With Plasma Cell Disorders

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06286215
Acronym
Registry PCD
Enrollment
750
Registered
2024-02-29
Start date
2024-04-01
Completion date
2035-04-01
Last updated
2024-02-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Plasma Cell Disorders

Keywords

registry, plasma cell disorder

Brief summary

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.

Interventions

None listed

Sponsors

Siriraj Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
register the plasma cell disorder patients10 yearsregister the plasma cell disorder patients

Secondary

MeasureTime frameDescription
incidence of plasma cell disorders10 yearsincidence of plasma cell disorders both before and after malignancy
Time to progression10 years\- 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 survival10 yearsProgression free survival
overall survival10 yearsoverall survival
influencing factors10 yearsfactors influencing overall survival, progression-free survival, and time to progression
Symptoms and signs10 yearsSymptoms and signs of the disease during the diagnosis and relapse phases, including the causes of mortality in plasma cell disorder patients
genetic characteristics10 yearsgenetic characteristics of plasma cell disorder
cost-effectiveness10 yearscost-effectiveness of treatment in Thailand

Contacts

Primary ContactChutima Kunacheewa, MD
chutima.kua@mahidol.ac.th66896790959
Backup ContactWeerapat Owatthanapanich, MD
weerapat.owa@mahidol.ac.th66891081983

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026