ID

13247

Beschreibung

AG-013736 (Axitinib) In Patients With Poor Prognosis Acute Myeloid Leukemia (AML) Or Myelodysplastic Syndrome (MDS); ODM derived from: https://clinicaltrials.gov/show/NCT00071006

Link

https://clinicaltrials.gov/show/NCT00071006

Stichworte

  1. 26.01.16 26.01.16 -
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CC BY-NC 3.0

Hochgeladen am

26. Januar 2016

DOI

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Creative Commons BY-NC 3.0

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Eligibility Acute Myeloid Leukemia (AML) NCT00071006

Eligibility Acute Myeloid Leukemia (AML) NCT00071006

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
poor prognosis aml or mds
Beschreibung

AML or MDS

Datentyp

boolean

Alias
UMLS CUI [1]
C0023467
UMLS CUI [2]
C3463824
histological confirmation of diagnosis
Beschreibung

histological confirmation

Datentyp

boolean

Alias
UMLS CUI [1]
C0019638
white blood cell count less than or equal to 30,000/mm3
Beschreibung

leukocytes

Datentyp

boolean

Alias
UMLS CUI [1]
C0023508
adequate hepatic and renal function documented within 14 days prior to registration
Beschreibung

hepatic and renal function

Datentyp

boolean

Alias
UMLS CUI [1]
C0232741
UMLS CUI [2]
C0232804
eastern cooperative oncology group (ecog) performance status of 0, 1, or 2
Beschreibung

ECOG

Datentyp

boolean

Alias
UMLS CUI [1]
C1520224
no evidence of preexisting uncontrolled hypertension
Beschreibung

hypertension

Datentyp

boolean

Alias
UMLS CUI [1]
C0020538
not a suitable candidate for chemotherapy
Beschreibung

not a suitable candidate for chemotherapy

Datentyp

boolean

Alias
UMLS CUI [1]
C0392920
no prior systemic chemotherapy treatment for aml or mds or treatment with an anti-angiogenesis agent
Beschreibung

no prior chemotherapy

Datentyp

boolean

Alias
UMLS CUI [1]
C0392920
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
candidate for chemotherapy
Beschreibung

candidate for chemotherapy

Datentyp

boolean

Alias
UMLS CUI [1]
C0392920
patients with aml m3 (acute promyelocytic leukemia)
Beschreibung

APL

Datentyp

boolean

Alias
UMLS CUI [1]
C0023487
conditions that might confound the evaluation of safety or efficacy or increase patient risk.
Beschreibung

conditions that might confound the evaluation of safety or efficacy or increase patient risk.

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2348563
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488

Ähnliche Modelle

Eligibility Acute Myeloid Leukemia (AML) NCT00071006

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
AML or MDS
Item
poor prognosis aml or mds
boolean
C0023467 (UMLS CUI [1])
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])
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])
Item Group
C0680251 (UMLS CUI)
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])

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