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NCT02869256 Clinical Trial

Regional Central Database Recording of Chronic Myeloid Leukemia

Chronic Myeloid Leukemia Clinical Trial

— LMC  

Official title:
Regional Central Database Recording of Chronic Myeloid Leukemia

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02869256
Other study ID # IB2014-LMC
Secondary ID
Status Recruiting
Phase N/A
First received August 9, 2016
Last updated November 17, 2017
Start date January 2014
Est. completion date January 2024

Study information
Verified date November 2017
Source Institut Bergonié
Contact Gabriel etienne, MD
Email G.Etienne@bordeaux.unicancer.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

It will be a centralized database , multicentre (6 centers) , regional, chronic myelogenous leukemia cases of registration (CML) prospectively and retrospectively.

Description:

Given the complexity and evolution of recommendations and to harmonize these, it appears necessary to establish a central database for recording , monitoring patients with CML supported by the participating centers the region and evaluation of care practices in use .

Indeed , the main purpose of this database is to provide diagnostic and therapeutic management of reported cases of chronic myeloid leukemia and to study the prognostic factors . The main objective is to improve significantly the percentage of patients treated adequately load in the region, in the initial stages of the disease and during its evolution.

Recruitment information / eligibility
Status Recruiting
Enrollment 400
Est. completion date January 2024
Est. primary completion date January 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- chronic myeloid leukemia Diagnosis (CML) in chronic phase , accelerated or blast

- male or female patient aged 18 years or more

- Cases transmitted by referring hematologist , one of the 6 participating centers after patient's oral information

- Clinical record presented Concertation Meeting LMC Multidisciplinary coordinated by the Institute Bergonié

Exclusion Criteria:

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Practices evaluation
Practices evaluation

Locations
Country Name City State
France Centre Hospitalier Universitaire de Bordeaux Bordeaux
France Institut Bergonié Bordeaux
France Polyclinique Bordeaux Nord Bordeaux
France Centre Hospitalier Universitaire de Dax Dax
France Centre hospitalier Libourne Libourne
France Centre Hospitalier Universitaire de Pau Pau

Sponsors (1)
Lead Sponsor Collaborator
Institut Bergonié

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary compliance of the management of patients with chronic myeloid leukemia compared to the guidelines 10 years
Secondary overall survival 10 years
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