Trial Title:
Chronic Myeloid Leukemia (CML) Real-Life Database
NCT ID:
NCT05963061
Condition:
Chronic Myeloid Leukemia (CML)
Conditions: Official terms:
Leukemia
Leukemia, Myeloid
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
Conditions: Keywords:
Leukemia
Leukemia, Myeloid
Chronic myeloid leukemia
Chronic, BCR::ABL Positive
Hematologic Malignancies
Tyrosine kinase inhibitor (TKI)
Targeted therapy
Study type:
Observational [Patient Registry]
Overall status:
Recruiting
Study design:
Time perspective:
Other
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.
Detailed description:
Observational study collecting real-life clinico-biological data from patients with CML.
Data are collected prospectively and retrospectively, from diagnosis and throughout the
long-term follow-up of CML (follow up continues after treatment stopped).
Criteria for eligibility:
Study pop:
Any patient with a diagnose of CML
Sampling method:
Non-Probability Sample
Criteria:
Inclusion Criteria:
- Patient diagnosed for chronic myelocytic leukemia
Exclusion Criteria:
- CML allograft without TKI treatment
- Refusal or inability to sign the consent
Gender:
All
Minimum age:
N/A
Maximum age:
N/A
Healthy volunteers:
No
Locations:
Facility:
Name:
CH Annecy Genevois
Address:
City:
Annecy
Country:
France
Status:
Recruiting
Investigator:
Last name:
Anne Parry, MD
Email:
Sub-Investigator
Facility:
Name:
University Hospital, Caen
Address:
City:
Caen
Country:
France
Status:
Recruiting
Investigator:
Last name:
Atchroue Johnson Ansah, MD
Email:
Sub-Investigator
Facility:
Name:
CHU Clemront-Ferrand
Address:
City:
Clermont-Ferrand
Country:
France
Status:
Recruiting
Investigator:
Last name:
Marc Berger, MD
Email:
Principal Investigator
Facility:
Name:
Centre Hospitalier Emile Roux
Address:
City:
Le Puy-en-Velay
Country:
France
Status:
Recruiting
Investigator:
Last name:
Vanessa Pante, MD
Email:
Sub-Investigator
Facility:
Name:
University Hospital, Limoges
Address:
City:
Limoges
Country:
France
Status:
Recruiting
Investigator:
Last name:
Amelie Penot, MD
Email:
Sub-Investigator
Facility:
Name:
Institut Paoli-Calmettes
Address:
City:
Marseille
Country:
France
Status:
Recruiting
Investigator:
Last name:
Aude CHARBONNIER, MD
Email:
Sub-Investigator
Facility:
Name:
Centre Hospital, Nancy
Address:
City:
Nancy
Country:
France
Status:
Recruiting
Investigator:
Last name:
Agnès Guerci-Bresler, MD
Email:
Sub-Investigator
Facility:
Name:
Bicetre Hospital
Address:
City:
Paris
Country:
France
Status:
Recruiting
Investigator:
Last name:
Ali Turhan, MD
Email:
Sub-Investigator
Facility:
Name:
Hopital Paul Brousse
Address:
City:
Paris
Country:
France
Status:
Recruiting
Investigator:
Last name:
Laurence Legros, MD
Email:
Sub-Investigator
Facility:
Name:
Rennes University Hospital
Address:
City:
Rennes
Country:
France
Status:
Recruiting
Investigator:
Last name:
Martine Escoffre-Barbe, MD
Email:
Sub-Investigator
Facility:
Name:
Centre Hospitalier de Rochefort
Address:
City:
Rochefort
Country:
France
Status:
Recruiting
Investigator:
Last name:
Guillaume DENIS, MD
Email:
Sub-Investigator
Facility:
Name:
Centre Hospitalier Universitaire de Saint Etienne
Address:
City:
Saint-Étienne
Country:
France
Status:
Recruiting
Investigator:
Last name:
Denis Guyotat, MD
Email:
Sub-Investigator
Facility:
Name:
University Hospital, Toulouse
Address:
City:
Toulouse
Country:
France
Status:
Recruiting
Investigator:
Last name:
Françoise Huguet, MD
Email:
Sub-Investigator
Facility:
Name:
Versailles Hospital
Address:
City:
Versailles
Country:
France
Status:
Recruiting
Investigator:
Last name:
Philippe Rousselot, MD
Email:
Sub-Investigator
Start date:
April 16, 2014
Completion date:
April 16, 2034
Lead sponsor:
Agency:
University Hospital, Clermont-Ferrand
Agency class:
Other
Collaborator:
Agency:
Centre Hospitalier Universitaire de Saint Etienne
Agency class:
Other
Collaborator:
Agency:
Bicetre Hospital
Agency class:
Other
Collaborator:
Agency:
University Hospital, Caen
Agency class:
Other
Collaborator:
Agency:
Central Hospital, Nancy, France
Agency class:
Other
Collaborator:
Agency:
University Hospital, Toulouse
Agency class:
Other
Collaborator:
Agency:
CH Annecy Genevois
Agency class:
Other
Collaborator:
Agency:
Rennes University Hospital
Agency class:
Other
Collaborator:
Agency:
Hopital Paul Brousse
Agency class:
Other
Collaborator:
Agency:
Versailles Hospital
Agency class:
Other
Collaborator:
Agency:
Centre Hospitalier Emile Roux
Agency class:
Other
Collaborator:
Agency:
University Hospital, Limoges
Agency class:
Other
Collaborator:
Agency:
Institut Paoli-Calmettes
Agency class:
Other
Collaborator:
Agency:
Centre Hospitalier de Rochefort
Agency class:
Other
Source:
University Hospital, Clermont-Ferrand
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05963061
https://link.springer.com/article/10.1007/s00277-022-04955-z
