ID

13578

Beskrivning

Standard vs. Reduced-Intensity Conditioning in Patients With Acute Myeloid Leukemia in First Remission; ODM derived from: https://clinicaltrials.gov/show/NCT00150878

Länk

https://clinicaltrials.gov/show/NCT00150878

Nyckelord

  1. 2016-02-17 2016-02-17 -
Rättsinnehavare

CC BY-NC 3.0

Uppladdad den

17 februari 2016

DOI

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Licens

Creative Commons BY-NC 3.0

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Eligibility Acute Myeloid Leukemia NCT00150878

Eligibility Acute Myeloid Leukemia NCT00150878

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis of acute myeloid leukemia in first remission
Beskrivning

diagnosis of acute myeloid leukemia in first remission

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0153886
UMLS CUI [1,2]
C0205435
standard-or high-risk marrow cytogenetics
Beskrivning

standard-or high-risk marrow cytogenetics

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0010802
UMLS CUI [1,2]
C0005953
UMLS CUI [1,3]
C0086930
hla-matched related or unrelated donor available (in case of high-risk disease)
Beskrivning

hla-matched related or unrelated donor available (in case of high-risk disease)

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0013018
UMLS CUI [1,2]
C2348930
age 18 to 60
Beskrivning

age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
informed consent
Beskrivning

informed consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
consent of donor to donate peripheral blood stem cells
Beskrivning

consent of donor to donate peripheral blood stem cells

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0013018
UMLS CUI [1,3]
C1518999
sufficient liver function (elevation of transferases < 2.5 x upper limit)
Beskrivning

sufficient liver function (elevation of transferases < 2.5 x upper limit)

Datatyp

boolean

Alias
UMLS CUI [1]
C0040676
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
aml with t(5;17)
Beskrivning

aml with t(5;17)

Datatyp

boolean

Alias
UMLS CUI [1]
C0023467
aml with t((8;21)
Beskrivning

aml with t((8;21)

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0023467
UMLS CUI [1,2]
C3897139
clinically relevant heart failure (nyha ii-iv)
Beskrivning

clinically relevant heart failure (nyha ii-iv)

Datatyp

boolean

Alias
UMLS CUI [1]
C1275491
renal failure (creatinine > 200 µg/ml)
Beskrivning

renal failure (creatinine > 200 µg/ml)

Datatyp

boolean

Alias
UMLS CUI [1]
C0201976
liver function failure (bilirubin > 3 mg/dl)
Beskrivning

liver function failure (bilirubin > 3 mg/dl)

Datatyp

boolean

Alias
UMLS CUI [1]
C1278039
concomitant neurological or psychiatric disease
Beskrivning

concomitant neurological or psychiatric disease

Datatyp

boolean

Alias
UMLS CUI [1]
C0009488
contraindications to receive prescribed study medication
Beskrivning

contraindications to receive prescribed study medication

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0013227
hiv infection
Beskrivning

hiv infection

Datatyp

boolean

Alias
UMLS CUI [1]
C0019693
pregnancy
Beskrivning

pregnancy

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961

Similar models

Eligibility Acute Myeloid Leukemia NCT00150878

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
AML in first remission
Item
diagnosis of acute myeloid leukemia in first remission
boolean
C0153886 (UMLS CUI [1,1])
C0205435 (UMLS CUI [1,2])
marrow cytogenetics
Item
standard-or high-risk marrow cytogenetics
boolean
C0010802 (UMLS CUI [1,1])
C0005953 (UMLS CUI [1,2])
C0086930 (UMLS CUI [1,3])
HLA-matched donor
Item
hla-matched related or unrelated donor available (in case of high-risk disease)
boolean
C0013018 (UMLS CUI [1,1])
C2348930 (UMLS CUI [1,2])
age
Item
age 18 to 60
boolean
C0001779 (UMLS CUI [1])
informed consent
Item
informed consent
boolean
C0021430 (UMLS CUI [1])
peripheral blood stem cells
Item
consent of donor to donate peripheral blood stem cells
boolean
C0021430 (UMLS CUI [1,1])
C0013018 (UMLS CUI [1,2])
C1518999 (UMLS CUI [1,3])
liver function
Item
sufficient liver function (elevation of transferases < 2.5 x upper limit)
boolean
C0040676 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
aml with t(5;17)
Item
aml with t(5;17)
boolean
C0023467 (UMLS CUI [1])
aml with t((8;21)
Item
aml with t((8;21)
boolean
C0023467 (UMLS CUI [1,1])
C3897139 (UMLS CUI [1,2])
heart failure
Item
clinically relevant heart failure (nyha ii-iv)
boolean
C1275491 (UMLS CUI [1])
renal failure (creatinine > 200 µg/ml)
Item
renal failure (creatinine > 200 µg/ml)
boolean
C0201976 (UMLS CUI [1])
liver function failure (bilirubin > 3 mg/dl)
Item
liver function failure (bilirubin > 3 mg/dl)
boolean
C1278039 (UMLS CUI [1])
concomitant neurological or psychiatric disease
Item
concomitant neurological or psychiatric disease
boolean
C0009488 (UMLS CUI [1])
contraindications to receive prescribed study medication
Item
contraindications to receive prescribed study medication
boolean
C1301624 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
hiv infection
Item
hiv infection
boolean
C0019693 (UMLS CUI [1])
pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])

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