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Informatie:
Fout:
ID
21417
Beschrijving
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
Trefwoorden
Versies (2)
- 20-04-17 20-04-17 -
- 20-04-17 20-04-17 -
Geüploaded op
20 april 2017
DOI
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Licentie
Creative Commons BY-NC 3.0
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Eligibility Leukemia NCT00896766
Eligibility Leukemia NCT00896766
- StudyEvent: Eligibility
Similar models
Eligibility Leukemia NCT00896766
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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])
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])
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])
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])
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])
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])
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])
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])
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])