RecruitingNCT06956755
Registry of Myelodysplastic Syndromes and Therapy-related Acute Myeloid Leukemia
Sponsor
Groupe Francophone des Myelodysplasies
Enrollment
6,990 participants
Start Date
Jul 7, 2003
Study Type
OBSERVATIONAL
Conditions
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
Eligibility
Min Age: 18 Years
Plain Language Summary
Simplified for easier understanding
This is a registry study — a large database — for people diagnosed with myelodysplastic syndromes (MDS) or therapy-related acute myeloid leukemia (t-AML). These are blood cancers where blood cells do not develop properly, often as a result of previous cancer treatment. The registry will collect clinical information over time to better understand these conditions and improve care.
**You may be eligible if...**
- You are over 18 years old
- You have been diagnosed with MDS or therapy-related AML
- You are willing and able to provide written consent
**You may NOT be eligible if...**
- You are under 18 years old
- You are unwilling or unable to give informed consent
Talk to your doctor to see if this trial is right for you.
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06956755
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