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NCT02607059 Clinical Trial

Epidemiologic Registry PETHEMA LMA 2015

AML Clinical Trial

Official title:
Epidemiologic Registry of Patients Diagnosed With Acute Myeloid Leukemia (PETHEMA LMA 2015)

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02607059
Other study ID # LAM 2015
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 2015
Est. completion date December 2021

Study information
Verified date March 2021
Source PETHEMA Foundation
Contact Pau Montesinos, Dr
Email montesinos_pau@gva.es
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Epidemiologic and retrospective multicenter registry of all patients diagnosed with de novo or secondary acute myeloid leukemia (AML) in the PETHEMA Group institutions. This study is a non-interventional research regarding diagnosis and therapeutic approach

Description:

To perform this registry, every patient diagnosed with AML in the participant institutions, regardless type of AML and treatment administered, must be reported. It will be required to registry the main characteristics of the patients and AML at diagnosis, as cytomorphologic, immunophenotypic, and cytogenetic results, according to the habitual practice of the centers. The treatment which has been administered by every center of the PETHEMA Group, even when it is considered as supportive care, and evolution of the disease will also be reported (relapse o death). PETHEMA Group will input all the reported information in data bases

Recruitment information / eligibility
Status Recruiting
Enrollment 500
Est. completion date December 2021
Est. primary completion date December 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients diagnosed with acute myeloid leukemia Exclusion Criteria: - No exclusion criteria

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Registry

Locations
Country Name City State
Spain Hospital La Fe Valencia

Sponsors (1)
Lead Sponsor Collaborator
PETHEMA Foundation

Country where clinical trial is conducted

Spain, 

Outcome
Type Measure Description Time frame Safety issue
Primary characteristics of the patients diagnosed of AML 3 years
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