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Information:
Fel:
ID
17842
Beskrivning
Dexamethasone Compared With Prednisone During Induction Therapy and Methotrexate With or Without Leucovorin During Maintenance Therapy in Treating Patients With Newly Diagnosed High-Risk Acute Lymphoblastic Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT00075725
Länk
https://clinicaltrials.gov/show/NCT00075725
Nyckelord
Versioner (2)
- 2016-10-05 2016-10-05 -
- 2016-10-05 2016-10-05 -
Uppladdad den
5 oktober 2016
DOI
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Licens
Creative Commons BY-NC 3.0
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Eligibility Leukemia NCT00075725
Eligibility Leukemia NCT00075725
- StudyEvent: Eligibility
Similar models
Eligibility Leukemia NCT00075725
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Precursor B-lymphoblastic leukaemia acute
Item
newly diagnosed b-precursor acute lymphoblastic leukemia
boolean
C1737235 (UMLS CUI [1])
White Blood Cell Count procedure | Age
Item
wbc > 50,000/mm^3 for patients age 1 to 9
boolean
C0023508 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0001779 (UMLS CUI [2])
White Blood Cell Count procedure | Age | Steroid therapy | Testicular Disease
Item
any wbc for patients age 10 to 30 or patients who have received prior steroid therapy or patients with testicular disease
boolean
C0023508 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0149783 (UMLS CUI [3])
C0039584 (UMLS CUI [4])
C0001779 (UMLS CUI [2])
C0149783 (UMLS CUI [3])
C0039584 (UMLS CUI [4])
ALL Clinical Trial classification eligible | ALL Clinical Trial classification Enrollment
Item
must be eligible for and enrolled on classification study cog-aall03b1
boolean
C0023449 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0683326 (UMLS CUI [1,3])
C1548635 (UMLS CUI [1,4])
C0023449 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C0683326 (UMLS CUI [2,3])
C1516879 (UMLS CUI [2,4])
C0008976 (UMLS CUI [1,2])
C0683326 (UMLS CUI [1,3])
C1548635 (UMLS CUI [1,4])
C0023449 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C0683326 (UMLS CUI [2,3])
C1516879 (UMLS CUI [2,4])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Age
Item
1 to under 31
boolean
C0001779 (UMLS CUI [1])
performance status
Item
performance status
boolean
C1518965 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Life Expectancy
Item
life expectancy
boolean
C0023671 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Function Hematopoietic
Item
hematopoietic
boolean
C0031843 (UMLS CUI [1,1])
C0229601 (UMLS CUI [1,2])
C0229601 (UMLS CUI [1,2])
disease characteristic
Item
see disease characteristics
boolean
C0599878 (UMLS CUI [1])
Liver function
Item
hepatic
boolean
C0232741 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Renal function
Item
renal
boolean
C0232804 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Prior Therapy
Item
prior concurrent therapy:
boolean
C1514463 (UMLS CUI [1])
Biological treatment
Item
biologic therapy
boolean
C1531518 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Chemotherapy
Item
chemotherapy
boolean
C0392920 (UMLS CUI [1])
Cytarabine Intrathecal
Item
no more than 72 hours since prior intrathecal cytarabine
boolean
C0010711 (UMLS CUI [1,1])
C0677897 (UMLS CUI [1,2])
C0677897 (UMLS CUI [1,2])
Cytotoxic Chemotherapy
Item
no other prior cytotoxic chemotherapy
boolean
C0677881 (UMLS CUI [1])
Hormone Therapy
Item
endocrine therapy
boolean
C0279025 (UMLS CUI [1])
Steroids
Item
prior steroids allowed
boolean
C0038317 (UMLS CUI [1])
Therapeutic radiology procedure
Item
radiotherapy
boolean
C1522449 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Operative Surgical Procedures
Item
surgery
boolean
C0543467 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])