Information:
Fel:
ID
13247
Beskrivning
AG-013736 (Axitinib) In Patients With Poor Prognosis Acute Myeloid Leukemia (AML) Or Myelodysplastic Syndrome (MDS); ODM derived from: https://clinicaltrials.gov/show/NCT00071006
Länk
https://clinicaltrials.gov/show/NCT00071006
Nyckelord
Versioner (1)
- 2016-01-26 2016-01-26 -
Rättsinnehavare
CC BY-NC 3.0
Uppladdad den
26 januari 2016
DOI
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Licens
Creative Commons BY-NC 3.0
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Eligibility Acute Myeloid Leukemia (AML) NCT00071006
Eligibility Acute Myeloid Leukemia (AML) NCT00071006
- StudyEvent: Eligibility
Similar models
Eligibility Acute Myeloid Leukemia (AML) NCT00071006
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
AML or MDS
Item
poor prognosis aml or mds
boolean
C0023467 (UMLS CUI [1])
C3463824 (UMLS CUI [2])
C3463824 (UMLS CUI [2])
histological confirmation
Item
histological confirmation of diagnosis
boolean
C0019638 (UMLS CUI [1])
leukocytes
Item
white blood cell count less than or equal to 30,000/mm3
boolean
C0023508 (UMLS CUI [1])
hepatic and renal function
Item
adequate hepatic and renal function documented within 14 days prior to registration
boolean
C0232741 (UMLS CUI [1])
C0232804 (UMLS CUI [2])
C0232804 (UMLS CUI [2])
ECOG
Item
eastern cooperative oncology group (ecog) performance status of 0, 1, or 2
boolean
C1520224 (UMLS CUI [1])
hypertension
Item
no evidence of preexisting uncontrolled hypertension
boolean
C0020538 (UMLS CUI [1])
not a suitable candidate for chemotherapy
Item
not a suitable candidate for chemotherapy
boolean
C0392920 (UMLS CUI [1])
no prior chemotherapy
Item
no prior systemic chemotherapy treatment for aml or mds or treatment with an anti-angiogenesis agent
boolean
C0392920 (UMLS CUI [1])
candidate for chemotherapy
Item
candidate for chemotherapy
boolean
C0392920 (UMLS CUI [1])
APL
Item
patients with aml m3 (acute promyelocytic leukemia)
boolean
C0023487 (UMLS CUI [1])
conditions that might confound the evaluation of safety or efficacy or increase patient risk.
Item
conditions that might confound the evaluation of safety or efficacy or increase patient risk.
boolean
C2348563 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])