ID

21418

Description

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

Lien

https://clinicaltrials.gov/show/NCT00896766

Mots-clés

Versions (2)
  1. 20/04/2017 20/04/2017 -
  2. 20/04/2017 20/04/2017 -
Téléchargé le

20 avril 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Leukemia NCT00896766

Anglais

Eligibility Leukemia NCT00896766

1 Formulaires  
  1. StudyEvent: Eligibility
    1. Eligibility Leukemia NCT00896766
Criteria
Description

Criteria

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

Precursor B-cell lymphoblastic leukemia

Type de données

boolean

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

Disease High risk

Type de données

boolean

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

Participation Clinical Trial Specified

Type de données

boolean

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

In complete remission

Type de données

boolean

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

Consent Clinical Trials Tissue Banks Use of

Type de données

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)
Description

Participation Clinical Trials Specified

Type de données

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
Description

Bone Marrow Recurrent disease

Type de données

boolean

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

Consent Clinical Trials Tissue Banks Use of

Type de données

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
Description

Matched ALL Blast Specimen | Matched ALL Germline Specimen

Type de données

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
Description

Data Demographic Specimen | Clinical Data Specimen | Data Pathologic Specimen

Type de données

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:
Description

Client Characteristics

Type de données

boolean

Alias
UMLS CUI [1]
C0815172
not specified
Description

Unspecified

Type de données

boolean

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

Therapeutic procedure

Type de données

boolean

Alias
UMLS CUI [1]
C0087111
not specified
Description

Unspecified

Type de données

boolean

Alias
UMLS CUI [1]
C0205370
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Similar models

Eligibility Leukemia NCT00896766

1 Formulaires
  1. StudyEvent: Eligibility
    1. Eligibility Leukemia NCT00896766
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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])
Retour au début de la page 

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