Informatie:
Fout:
ID
13625
Beschrijving
AML96 - Risk-Adapted and Randomized Postremission-Therapy for Adult Acute Myeloid Leukemia Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00180115
Link
https://clinicaltrials.gov/show/NCT00180115
Trefwoorden
Versies (1)
- 21-02-16 21-02-16 -
Geüploaded op
21 februari 2016
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Leukemia, Nonlymphoblastic, Acute NCT00180115
Eligibility Leukemia, Nonlymphoblastic, Acute NCT00180115
- StudyEvent: Eligibility
Similar models
Eligibility Leukemia, Nonlymphoblastic, Acute NCT00180115
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
AML of specific fab type
Item
de novo or secondary acute myeloid leukemia of the fab subtypes m0-m2 and m4-m7
boolean
C0023467 (UMLS CUI [1])
C0457321 (UMLS CUI [2])
C0457321 (UMLS CUI [2])
mds of specific fab type
Item
de novo or secondary myelodysplastic syndrome fab subtypes raeb and raeb-t
boolean
C3463824 (UMLS CUI [1])
C0457321 (UMLS CUI [2])
C0457321 (UMLS CUI [2])
informed consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
severe comorbidities
Item
severe comorbidities
boolean
C0009488 (UMLS CUI [1])
complications of the leukemia
Item
severe uncontrolled complications of the leukemia
boolean
C0544688 (UMLS CUI [1])
prior therapy
Item
previous therapy of leukemia/mds
boolean
C1514463 (UMLS CUI [1])
hiv
Item
hiv-infection
boolean
C0019682 (UMLS CUI [1])
allergy against study medication
Item
known relevant allergy against study medication
boolean
C0020517 (UMLS CUI [1,1])
C1521826 (UMLS CUI [1,2])
C1521826 (UMLS CUI [1,2])
pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
missing written informed consent
Item
missing written informed consent
boolean
C0021430 (UMLS CUI [1])