ID

21417

Descripción

Laboratory Study of Lymphoblasts in Young Patients With High-Risk Acute Lymphoblastic Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT00896766

Link

https://clinicaltrials.gov/show/NCT00896766

Palabras clave

Versiones (2)
  1. 20/4/17 20/4/17 -
  2. 20/4/17 20/4/17 -
Subido en

20 de abril de 2017

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY-NC 3.0
Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Volver a los comentarios del modelo
Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Eligibility Leukemia NCT00896766

Inglés

Eligibility Leukemia NCT00896766

1 formularios  
  1. StudyEvent: Eligibility
    1. Eligibility Leukemia NCT00896766
Criteria
Descripción

Criteria

diagnosis of b-cell precursor acute lymphoblastic leukemia (all)
Descripción

Precursor B-cell lymphoblastic leukemia

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1292769
high-risk disease
Descripción

Disease High risk

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0332167
participation in clinical trial cog-p9906 required (pilot project)
Descripción

Participation Clinical Trial Specified

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0679823
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C0205369
in complete remission
Descripción

In complete remission

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0677874
consented to future studies using banked tissue specimens
Descripción

Consent Clinical Trials Tissue Banks Use of

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1511481
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C0040278
UMLS CUI [1,4]
C1524063
participation in clinical trial and cog-aall03b1 and linked therapeutic studies cog-aall0232 and cog- aall0331(expansion project)
Descripción

Participation Clinical Trials Specified

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0679823
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C0205369
experienced a bone marrow relapse within 36 months of initial diagnosis
Descripción

Bone Marrow Recurrent disease

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0005953
UMLS CUI [1,2]
C0277556
consented to future studies using banked tissue specimens
Descripción

Consent Clinical Trials Tissue Banks Use of

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1511481
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C0040278
UMLS CUI [1,4]
C1524063
have matched all blast and germline specimens
Descripción

Matched ALL Blast Specimen | Matched ALL Germline Specimen

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1708943
UMLS CUI [1,2]
C0023449
UMLS CUI [1,3]
C0368761
UMLS CUI [1,4]
C0370003
UMLS CUI [2,1]
C1708943
UMLS CUI [2,2]
C0023449
UMLS CUI [2,3]
C3845275
UMLS CUI [2,4]
C0370003
demographic, clinical and pathologic data elements for these biospecimens available
Descripción

Data Demographic Specimen | Clinical Data Specimen | Data Pathologic Specimen

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1511726
UMLS CUI [1,2]
C0011298
UMLS CUI [1,3]
C0370003
UMLS CUI [2,1]
C1516606
UMLS CUI [2,2]
C0370003
UMLS CUI [3,1]
C1511726
UMLS CUI [3,2]
C1521733
UMLS CUI [3,3]
C0370003
patient characteristics:
Descripción

Client Characteristics

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0815172
not specified
Descripción

Unspecified

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0205370
prior concurrent therapy:
Descripción

Therapeutic procedure

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0087111
not specified
Descripción

Unspecified

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0205370
Volver a la parte superior de la página

Similar models

Eligibility Leukemia NCT00896766

1 formularios
  1. StudyEvent: Eligibility
    1. Eligibility Leukemia NCT00896766
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Precursor B-cell lymphoblastic leukemia
Item
diagnosis of b-cell precursor acute lymphoblastic leukemia (all)
boolean
C1292769 (UMLS CUI [1])
Disease High risk
Item
high-risk disease
boolean
C0012634 (UMLS CUI [1,1])
C0332167 (UMLS CUI [1,2])
Participation Clinical Trial Specified
Item
participation in clinical trial cog-p9906 required (pilot project)
boolean
C0679823 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
In complete remission
Item
in complete remission
boolean
C0677874 (UMLS CUI [1])
Consent Clinical Trials Tissue Banks Use of
Item
consented to future studies using banked tissue specimens
boolean
C1511481 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0040278 (UMLS CUI [1,3])
C1524063 (UMLS CUI [1,4])
Participation Clinical Trials Specified
Item
participation in clinical trial and cog-aall03b1 and linked therapeutic studies cog-aall0232 and cog- aall0331(expansion project)
boolean
C0679823 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
Bone Marrow Recurrent disease
Item
experienced a bone marrow relapse within 36 months of initial diagnosis
boolean
C0005953 (UMLS CUI [1,1])
C0277556 (UMLS CUI [1,2])
Consent Clinical Trials Tissue Banks Use of
Item
consented to future studies using banked tissue specimens
boolean
C1511481 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0040278 (UMLS CUI [1,3])
C1524063 (UMLS CUI [1,4])
Matched ALL Blast Specimen | Matched ALL Germline Specimen
Item
have matched all blast and germline specimens
boolean
C1708943 (UMLS CUI [1,1])
C0023449 (UMLS CUI [1,2])
C0368761 (UMLS CUI [1,3])
C0370003 (UMLS CUI [1,4])
C1708943 (UMLS CUI [2,1])
C0023449 (UMLS CUI [2,2])
C3845275 (UMLS CUI [2,3])
C0370003 (UMLS CUI [2,4])
Data Demographic Specimen | Clinical Data Specimen | Data Pathologic Specimen
Item
demographic, clinical and pathologic data elements for these biospecimens available
boolean
C1511726 (UMLS CUI [1,1])
C0011298 (UMLS CUI [1,2])
C0370003 (UMLS CUI [1,3])
C1516606 (UMLS CUI [2,1])
C0370003 (UMLS CUI [2,2])
C1511726 (UMLS CUI [3,1])
C1521733 (UMLS CUI [3,2])
C0370003 (UMLS CUI [3,3])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Volver a la parte superior de la página 

Contacto

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Ayuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial