ID

14533

Beschrijving

IFM 99-02 Thalidomide in Myeloma; ODM derived from: https://clinicaltrials.gov/show/NCT00222053

Link

https://clinicaltrials.gov/show/NCT00222053

Trefwoorden

  1. 19-04-16 19-04-16 -
Geüploaded op

19 april 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Multiple Myeloma NCT00222053

Eligibility Multiple Myeloma NCT00222053

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
de novo myeloma
Beschrijving

Myeloma

Datatype

boolean

Alias
UMLS CUI [1]
C0026764
according to durie and salmon classification stage ii, iii and stage i with a lytic bone lesion
Beschrijving

Durie and salmon classification

Datatype

boolean

Alias
UMLS CUI [1]
C0278722
UMLS CUI [2]
C02787223
UMLS CUI [3]
C0278724
patients from 18 to 65 years old
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
beta2microglobulin < 3 mg/l or del13 absent
Beschrijving

Beta2microglobulin or del13

Datatype

boolean

Alias
UMLS CUI [1]
C0201910
UMLS CUI [2]
C1517957
signed informed consent
Beschrijving

Informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
eligible for transplantation
Beschrijving

Transplantation eligible

Datatype

boolean

Alias
UMLS CUI [1,1]
C0040732
UMLS CUI [1,2]
C0013893
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
peripheral neurological toxicities
Beschrijving

Neurological toxicity

Datatype

boolean

Alias
UMLS CUI [1]
C0031117
uncontrolled or severe cardiovascular disease
Beschrijving

Cardiovascular disease

Datatype

boolean

Alias
UMLS CUI [1]
C0007222
other malignancy except basocellular carcinoma or figo stage i carcinoma of the cervix
Beschrijving

Further malignancies

Datatype

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0332196
UMLS CUI [1,3]
C0007114
UMLS CUI [2,1]
C0006826
UMLS CUI [2,2]
C0332196
UMLS CUI [2,3]
C2216722
patient who received biphosphonate during the last 60 days
Beschrijving

Biphosphonate

Datatype

boolean

Alias
UMLS CUI [1]
C0012544
renal failure definited as creatinine > 150 µmol/l
Beschrijving

Creatinine measurement

Datatype

boolean

Alias
UMLS CUI [1]
C0201976
patient with obvious vascular cerebral medical history
Beschrijving

Cerebrovascular disorder

Datatype

boolean

Alias
UMLS CUI [1]
C0007820
liver dysfunction definited as bilirubin > 35 µmol/l or asat, alat, pal > 4n
Beschrijving

Bilirubin, asat, alat, pal

Datatype

boolean

Alias
UMLS CUI [1]
C1278039
UMLS CUI [2]
C0201899
UMLS CUI [3]
C0201836
UMLS CUI [4]
C1278131
respiratory dysfunction
Beschrijving

Pulmonary function

Datatype

boolean

Alias
UMLS CUI [1]
C0231921
hiv +
Beschrijving

HIV positivity

Datatype

boolean

Alias
UMLS CUI [1]
C0019699
patient who refused to use an acceptable barrier method for contraception
Beschrijving

Contraception

Datatype

boolean

Alias
UMLS CUI [1]
C0700589

Similar models

Eligibility Multiple Myeloma NCT00222053

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Myeloma
Item
de novo myeloma
boolean
C0026764 (UMLS CUI [1])
Durie and salmon classification
Item
according to durie and salmon classification stage ii, iii and stage i with a lytic bone lesion
boolean
C0278722 (UMLS CUI [1])
C02787223 (UMLS CUI [2])
C0278724 (UMLS CUI [3])
Age
Item
patients from 18 to 65 years old
boolean
C0001779 (UMLS CUI [1])
Beta2microglobulin or del13
Item
beta2microglobulin < 3 mg/l or del13 absent
boolean
C0201910 (UMLS CUI [1])
C1517957 (UMLS CUI [2])
Informed consent
Item
signed informed consent
boolean
C0021430 (UMLS CUI [1])
Transplantation eligible
Item
eligible for transplantation
boolean
C0040732 (UMLS CUI [1,1])
C0013893 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Neurological toxicity
Item
peripheral neurological toxicities
boolean
C0031117 (UMLS CUI [1])
Cardiovascular disease
Item
uncontrolled or severe cardiovascular disease
boolean
C0007222 (UMLS CUI [1])
Further malignancies
Item
other malignancy except basocellular carcinoma or figo stage i carcinoma of the cervix
boolean
C0006826 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C0007114 (UMLS CUI [1,3])
C0006826 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])
C2216722 (UMLS CUI [2,3])
Biphosphonate
Item
patient who received biphosphonate during the last 60 days
boolean
C0012544 (UMLS CUI [1])
Creatinine measurement
Item
renal failure definited as creatinine > 150 µmol/l
boolean
C0201976 (UMLS CUI [1])
Cerebrovascular disorder
Item
patient with obvious vascular cerebral medical history
boolean
C0007820 (UMLS CUI [1])
Bilirubin, asat, alat, pal
Item
liver dysfunction definited as bilirubin > 35 µmol/l or asat, alat, pal > 4n
boolean
C1278039 (UMLS CUI [1])
C0201899 (UMLS CUI [2])
C0201836 (UMLS CUI [3])
C1278131 (UMLS CUI [4])
Pulmonary function
Item
respiratory dysfunction
boolean
C0231921 (UMLS CUI [1])
HIV positivity
Item
hiv +
boolean
C0019699 (UMLS CUI [1])
Contraception
Item
patient who refused to use an acceptable barrier method for contraception
boolean
C0700589 (UMLS CUI [1])

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