A "Physician & Patient-powered" Cohort Registry (MY MYELOMA)

NCT05001087 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1900

Last updated 2025-02-27

No results posted yet for this study

Summary

The aim of this observational study is the creation of a national multiple myeloma registry to monitor the current routine clinical practice in Italy and describe the standard of care adopted for the diagnosis and treatment of patients with multiple myeloma in the different Italian hematology centers.

Conditions

Interventions

OTHER

Observation

Not applicable-Observational study

Sponsors & Collaborators

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-03-16
Primary Completion
2027-03-31
Completion
2027-03-31

Countries

  • Italy

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05001087 on ClinicalTrials.gov