Informationen:
Fehler:
ID
14844
Beschreibung
A Study of the Histone-deacetylase Inhibitor JNJ-26481585 in Patients With Advanced or Refractory Leukemia or Myelodysplastic Syndrome; ODM derived from: https://clinicaltrials.gov/show/NCT00676728
Link
https://clinicaltrials.gov/show/NCT00676728
Stichworte
Versionen (1)
- 01.05.16 01.05.16 -
Hochgeladen am
1. Mai 2016
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Advanced or Refractory Leukemia NCT00676728
Eligibility Advanced or Refractory Leukemia NCT00676728
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Advanced or Refractory Leukemia NCT00676728
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
acute myeloid leukemia, acute lymphocytic leukemia
Item
histologically or cytologically confirmed advanced or refractory acute myeloid leukemia, acute lymphocytic leukemia, chronic myeloid leukemia in blast phase, refractory chronic lymphocytic leukemia, myelodysplastic syndrome, or chronic myelomonocytic leukemia
boolean
C0023440 (UMLS CUI [1])
C0023449 (UMLS CUI [2])
C0023449 (UMLS CUI [2])
myelodysplastic syndrome
Item
myelodysplastic syndrome
boolean
C3463824 (UMLS CUI [1])
ecog
Item
eastern cooperative oncology group performance status score 0, 1 or 2
boolean
C1520224 (UMLS CUI [1])
left ventricular ejection fraction
Item
left ventricular ejection fraction greater than or equal to 50%
boolean
C0428772 (UMLS CUI [1])
negative hepatitis b, c and human immunodeficiency virus (hiv)
Item
negative hepatitis b, c and human immunodeficiency virus (hiv) test within last 3 months
boolean
C2711110 (UMLS CUI [1])
C0019693 (UMLS CUI [2])
C0019693 (UMLS CUI [2])
liver and kidney function
Item
adequate liver and kidney function
boolean
C0232741 (UMLS CUI [1,1])
C0232804 (UMLS CUI [1,2])
C0232804 (UMLS CUI [1,2])
involvement of the central nervous system
Item
known or suspected involvement of the central nervous system
boolean
C0449389 (UMLS CUI [1])
chemotherapy, radiotherapy
Item
chemotherapy (nitrosoureas and mitomycin c within 6 weeks), radiotherapy, immunotherapy or treatment with investigative agent within 3 weeks before study drug administration (except hydroxyurea which should be stopped at least 24 hours prior to first dose)
boolean
C0392920 (UMLS CUI [1])
C1522449 (UMLS CUI [2])
C1522449 (UMLS CUI [2])
unstable angina or myocardial infarction, congestive heart failure
Item
unstable angina or myocardial infarction within the preceding 12 months; congestive heart failure
boolean
C0018802 (UMLS CUI [1])
C0027051 (UMLS CUI [2])
C0002965 (UMLS CUI [3])
C0027051 (UMLS CUI [2])
C0002965 (UMLS CUI [3])
hypertension or diabetes
Item
poorly controlled hypertension or diabetes, ongoing active infection and psychiatric illness
boolean
C0020538 (UMLS CUI [1])
C0020538 (UMLS CUI [2])
C0020538 (UMLS CUI [2])
qtc prolongation
Item
receiving medications known to have a risk of causing qtc prolongation
boolean