Registry of Myelodysplastic Syndromes and Therapy-related Acute Myeloid Leukemia

NCT06956755 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 6990

Last updated 2025-05-06

No results posted yet for this study

Summary

The Registry MDS is an ongoing, observational study that has collected longitudinal data on diagnostics, demographics, clinical parameters, and health Care Interventions (HCI) from patients with MDS and therapy-related acute myeloid leukemia

Conditions

Sponsors & Collaborators

  • Groupe Francophone des Myelodysplasies

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-07-07
Primary Completion
2030-01-05
Completion
2031-01-05

Countries

  • France

Study Locations

More Related Trials

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 NCT06956755 on ClinicalTrials.gov