ID

14836

Beschrijving

Total-Body Irradiation, Fludarabine, and Alemtuzumab Followed By Stem Cell Transplant in Treating Patients With Myeloproliferative Disorder, MS, AML, or CML; ODM derived from: https://clinicaltrials.gov/show/NCT00069992

Link

https://clinicaltrials.gov/show/NCT00069992

Trefwoorden

  1. 01-05-16 01-05-16 -
Geüploaded op

1 mei 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Chronic Myeloproliferative Disorders NCT00069992

Eligibility Chronic Myeloproliferative Disorders NCT00069992

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
myelodysplastic syndrome with ipss score > 0.(appendix b) or
Beschrijving

ID.1

Datatype

boolean

Alias
UMLS CUI [1]
C2827405
myeloproliferative disorders
Beschrijving

ID.2

Datatype

boolean

Alias
UMLS CUI [1]
C0027022
primary myelofibrosis with lile score of 1 or 2 (appendix c)
Beschrijving

ID.3

Datatype

boolean

Alias
UMLS CUI [1]
C0001815
polycythemia vera or essential thrombocythemia transformed to aml or myelofibrosis and pv "spent phase" or
Beschrijving

ID.4

Datatype

boolean

Alias
UMLS CUI [1]
C0032463
UMLS CUI [2]
C0040028
UMLS CUI [3]
C0023467
UMLS CUI [4]
C0001815
acute myelogenous leukemia or
Beschrijving

ID.5

Datatype

boolean

Alias
UMLS CUI [1]
C0023467
chronic myelogenous leukemia
Beschrijving

ID.6

Datatype

boolean

Alias
UMLS CUI [1]
C0023474
available healthy donor without any contraindications for donation. 5/6 or 6/6 related donor or 5/6 or 6/6 unrelated donor (molecular typing for drb1)
Beschrijving

ID.7

Datatype

boolean

Alias
UMLS CUI [1,1]
C0013018
UMLS CUI [1,2]
C0470187
able to give informed consent
Beschrijving

ID.8

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient is pregnant or lactating or unwilling to use contraceptives.
Beschrijving

ID.9

Datatype

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0006147
UMLS CUI [1,3]
C0700589
hiv positive patient
Beschrijving

ID.10

Datatype

boolean

Alias
UMLS CUI [1]
C0019682
uncontrolled intercurrent infection
Beschrijving

ID.11

Datatype

boolean

Alias
UMLS CUI [1]
C0009450
unstable angina and uncompensated congestive heart failure (zubrod of 3 or greater)
Beschrijving

ID.12

Datatype

boolean

Alias
UMLS CUI [1]
C0002965
UMLS CUI [2]
C0018802
severe chronic pulmonary disease requiring oxygen (zubrod of 3 or greater)
Beschrijving

ID.13

Datatype

boolean

Alias
UMLS CUI [1,1]
C0746102
UMLS CUI [1,2]
C0205082
hemodialysis dependent.
Beschrijving

ID.14

Datatype

boolean

Alias
UMLS CUI [1]
C0019004
active hepatitis or cirrhosis with total bilirubin, sgot, and sgpt greater than 3 x normal.
Beschrijving

ID.15

Datatype

boolean

Alias
UMLS CUI [1,1]
C0201899
UMLS CUI [1,2]
C0201836
UMLS CUI [1,3]
C1278039
concurrent solid organ malignancy not in remission, except for stage 0 or a prostate cancer.
Beschrijving

ID.16

Datatype

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0009488
unstable cerebral vascular disease or recent hemorrhagic stroke (less than 6 months)
Beschrijving

ID.17

Datatype

boolean

Alias
UMLS CUI [1]
C0007820
active cns disease from hematological disorder.
Beschrijving

ID.18

Datatype

boolean

Alias
UMLS CUI [1,1]
C0007682
UMLS CUI [1,2]
C0018939

Similar models

Eligibility Chronic Myeloproliferative Disorders NCT00069992

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
myelodysplastic syndrome with ipss score > 0.(appendix b) or
boolean
C2827405 (UMLS CUI [1])
ID.2
Item
myeloproliferative disorders
boolean
C0027022 (UMLS CUI [1])
ID.3
Item
primary myelofibrosis with lile score of 1 or 2 (appendix c)
boolean
C0001815 (UMLS CUI [1])
ID.4
Item
polycythemia vera or essential thrombocythemia transformed to aml or myelofibrosis and pv "spent phase" or
boolean
C0032463 (UMLS CUI [1])
C0040028 (UMLS CUI [2])
C0023467 (UMLS CUI [3])
C0001815 (UMLS CUI [4])
ID.5
Item
acute myelogenous leukemia or
boolean
C0023467 (UMLS CUI [1])
ID.6
Item
chronic myelogenous leukemia
boolean
C0023474 (UMLS CUI [1])
ID.7
Item
available healthy donor without any contraindications for donation. 5/6 or 6/6 related donor or 5/6 or 6/6 unrelated donor (molecular typing for drb1)
boolean
C0013018 (UMLS CUI [1,1])
C0470187 (UMLS CUI [1,2])
ID.8
Item
able to give informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
ID.9
Item
patient is pregnant or lactating or unwilling to use contraceptives.
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
C0700589 (UMLS CUI [1,3])
ID.10
Item
hiv positive patient
boolean
C0019682 (UMLS CUI [1])
ID.11
Item
uncontrolled intercurrent infection
boolean
C0009450 (UMLS CUI [1])
ID.12
Item
unstable angina and uncompensated congestive heart failure (zubrod of 3 or greater)
boolean
C0002965 (UMLS CUI [1])
C0018802 (UMLS CUI [2])
ID.13
Item
severe chronic pulmonary disease requiring oxygen (zubrod of 3 or greater)
boolean
C0746102 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
ID.14
Item
hemodialysis dependent.
boolean
C0019004 (UMLS CUI [1])
ID.15
Item
active hepatitis or cirrhosis with total bilirubin, sgot, and sgpt greater than 3 x normal.
boolean
C0201899 (UMLS CUI [1,1])
C0201836 (UMLS CUI [1,2])
C1278039 (UMLS CUI [1,3])
ID.16
Item
concurrent solid organ malignancy not in remission, except for stage 0 or a prostate cancer.
boolean
C0006826 (UMLS CUI [1,1])
C0009488 (UMLS CUI [1,2])
ID.17
Item
unstable cerebral vascular disease or recent hemorrhagic stroke (less than 6 months)
boolean
C0007820 (UMLS CUI [1])
ID.18
Item
active cns disease from hematological disorder.
boolean
C0007682 (UMLS CUI [1,1])
C0018939 (UMLS CUI [1,2])

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