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

Inclusion Criteria1

  • Patient diagnosed for chronic myelocytic leukemia

Exclusion Criteria2

  • CML allograft without TKI treatment
  • Refusal or inability to sign the consent

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