ID

12813

Beschrijving

Haplo-identical HSCT Versus Chemotherapy for Adult Acute Lymphoblastic Leukemia Patients; ODM derived from: https://clinicaltrials.gov/show/NCT02042690

Link

https://clinicaltrials.gov/show/NCT02042690

Trefwoorden

  1. 21-12-15 21-12-15 -
Geüploaded op

21 december 2015

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Acute Lymphoblastic Leukemia NCT02042690

Eligibility Acute Lymphoblastic Leukemia NCT02042690

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
acute lymphoblastic leukemia
Beschrijving

all

Datatype

boolean

Alias
UMLS CUI [1]
C0023449
18-39 years old
Beschrijving

age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
in first complete remission
Beschrijving

complete remission

Datatype

boolean

Alias
UMLS CUI [1]
C0677874
adequate hepatic function defined as: total bilirubin ≤2.0 times the institutional upper limit of normal (uln); alanine aminotransferase (alt) and aspartate aminotransferase(ast) ≤2.5 times the institutional uln -
Beschrijving

liver function

Datatype

boolean

Alias
UMLS CUI [1]
C0232741
adequate renal function defined as creatinine ≤3 times the institutional uln
Beschrijving

renal function

Datatype

boolean

Alias
UMLS CUI [1]
C0232804
no uncontrollable infection
Beschrijving

infection

Datatype

boolean

Alias
UMLS CUI [1]
C0009450
performance status(ps)score 0-2(who)
Beschrijving

who performance score

Datatype

boolean

Alias
UMLS CUI [1]
C1298650
subjects able to provide written informed consent
Beschrijving

informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
having hla-matched donor
Beschrijving

stem cell donor

Datatype

boolean

Alias
UMLS CUI [1]
C0375877
high-risk all: (1)ph+all (2)hypodiploidy (3)t(v;11q23) (4) complex karyotype(≥5 chromosome abnormalities)(5)high white blood cell (wbc) count (b-all≥30×109/l;t-all ≥100×109/l).
Beschrijving

high-risk all

Datatype

boolean

Alias
UMLS CUI [1]
C0684030
UMLS CUI [2]
C0023449
pregnancy
Beschrijving

pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0549206
loss of ability to freely provide consent due to psychiatric or physical illness
Beschrijving

limited informed consent due to comorbidity

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2]
C0439801
UMLS CUI [3]
C0009488

Similar models

Eligibility Acute Lymphoblastic Leukemia NCT02042690

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
all
Item
acute lymphoblastic leukemia
boolean
C0023449 (UMLS CUI [1])
age
Item
18-39 years old
boolean
C0001779 (UMLS CUI [1])
complete remission
Item
in first complete remission
boolean
C0677874 (UMLS CUI [1])
liver function
Item
adequate hepatic function defined as: total bilirubin ≤2.0 times the institutional upper limit of normal (uln); alanine aminotransferase (alt) and aspartate aminotransferase(ast) ≤2.5 times the institutional uln -
boolean
C0232741 (UMLS CUI [1])
renal function
Item
adequate renal function defined as creatinine ≤3 times the institutional uln
boolean
C0232804 (UMLS CUI [1])
infection
Item
no uncontrollable infection
boolean
C0009450 (UMLS CUI [1])
who performance score
Item
performance status(ps)score 0-2(who)
boolean
C1298650 (UMLS CUI [1])
informed consent
Item
subjects able to provide written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
stem cell donor
Item
having hla-matched donor
boolean
C0375877 (UMLS CUI [1])
high-risk all
Item
high-risk all: (1)ph+all (2)hypodiploidy (3)t(v;11q23) (4) complex karyotype(≥5 chromosome abnormalities)(5)high white blood cell (wbc) count (b-all≥30×109/l;t-all ≥100×109/l).
boolean
C0684030 (UMLS CUI [1])
C0023449 (UMLS CUI [2])
pregnancy
Item
pregnancy
boolean
C0549206 (UMLS CUI [1])
limited informed consent due to comorbidity
Item
loss of ability to freely provide consent due to psychiatric or physical illness
boolean
C0021430 (UMLS CUI [1])
C0439801 (UMLS CUI [2])
C0009488 (UMLS CUI [3])

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