RecruitingNCT05963061

Chronic Myeloid Leukemia (CML) Real-Life Database


Sponsor

University Hospital, Clermont-Ferrand

Enrollment

3,500 participants

Start Date

Apr 16, 2014

Study Type

OBSERVATIONAL

Conditions

Summary

Establish the largest possible real-life cohort collecting long-term follow-up of a maximum number of CML patients in order to carry out observational studies: epidemiological, identification of subgroups according to their response to treatment, evaluation of new molecules in real life, therapeutic discontinuations, impact of the evolution of recommendations, etc.


Eligibility

Plain Language Summary

Simplified for easier understanding

This study is building a real-world registry (a large database) to track patients with chronic myeloid leukemia (CML) — a type of blood cancer — over time, to better understand how the disease progresses and how patients respond to treatment in everyday clinical settings. **You may be eligible if...** - You have been diagnosed with chronic myeloid leukemia (CML) - You are willing and able to sign a consent form **You may NOT be eligible if...** - You have had a bone marrow transplant (allograft) for CML without receiving tyrosine kinase inhibitor (TKI) treatment - You refuse or are 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(14)

CH Annecy Genevois

Annecy, France

University Hospital, Caen

Caen, France

CHU Clemront-Ferrand

Clermont-Ferrand, France

Centre Hospitalier Emile Roux

Le Puy-en-Velay, France

University Hospital, Limoges

Limoges, France

Institut Paoli-Calmettes

Marseille, France

Centre Hospital, Nancy

Nancy, France

Bicetre Hospital

Paris, France

Hopital Paul Brousse

Paris, France

Rennes University Hospital

Rennes, France

Centre Hospitalier de Rochefort

Rochefort, France

Centre Hospitalier Universitaire de Saint Etienne

Saint-Etienne, France

University Hospital, Toulouse

Toulouse, France

Versailles Hospital

Versailles, France

View Full Details on ClinicalTrials.gov

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NCT05963061


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