ID

23242

Beskrivning

Thalidomide Versus Bortezomib in Melphalan Refractory Myeloma; ODM derived from: https://clinicaltrials.gov/show/NCT00602511

Länk

https://clinicaltrials.gov/show/NCT00602511

Nyckelord

  1. 2017-06-30 2017-06-30 -
Uppladdad den

30 juni 2017

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Multiple Myeloma NCT00602511

Eligibility Multiple Myeloma NCT00602511

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
treatment demanding multiple myeloma
Beskrivning

ID.1

Datatyp

boolean

Alias
UMLS CUI [1]
C0026764
refractoriness to melphalan
Beskrivning

ID.2

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0025241
UMLS CUI [1,2]
C0205269
acceptance of rules for prevention of pregnancy
Beskrivning

ID.3

Datatyp

boolean

Alias
UMLS CUI [1]
C0009862
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
previous treatment with bortezomib, thalidomide, or lenalidomide
Beskrivning

ID.4

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1176309
UMLS CUI [1,2]
C0039736
UMLS CUI [1,3]
C1144149
sensory neuropathy grade iii or neuropathic pain grade ii
Beskrivning

ID.5

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0151313
UMLS CUI [1,2]
C0003892
severe concomitant disorder, e.g. other malignancy or severe heart disease
Beskrivning

ID.6

Datatyp

boolean

Alias
UMLS CUI [1]
C0012634
transformation to plasma cell leukemia or aggressive lymphoma
Beskrivning

ID.7

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0023484
UMLS CUI [1,2]
C0024299
UMLS CUI [1,3]
C0580822
frequent visits for bortezomib injections not feasible
Beskrivning

ID.8

Datatyp

boolean

Alias
UMLS CUI [1]
C4276228
anticipated non-adherence to study protocol
Beskrivning

ID.9

Datatyp

boolean

Alias
UMLS CUI [1]
C1321605
pregnancy
Beskrivning

ID.10

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
anticipated non-adherence to rules for prevention of pregnancy
Beskrivning

ID.11

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0032961
severe thrombocytopenia (thrombocyte count less than 25000/microliter)
Beskrivning

ID.12

Datatyp

boolean

Alias
UMLS CUI [1]
C0040034

Similar models

Eligibility Multiple Myeloma NCT00602511

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
treatment demanding multiple myeloma
boolean
C0026764 (UMLS CUI [1])
ID.2
Item
refractoriness to melphalan
boolean
C0025241 (UMLS CUI [1,1])
C0205269 (UMLS CUI [1,2])
ID.3
Item
acceptance of rules for prevention of pregnancy
boolean
C0009862 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
ID.4
Item
previous treatment with bortezomib, thalidomide, or lenalidomide
boolean
C1176309 (UMLS CUI [1,1])
C0039736 (UMLS CUI [1,2])
C1144149 (UMLS CUI [1,3])
ID.5
Item
sensory neuropathy grade iii or neuropathic pain grade ii
boolean
C0151313 (UMLS CUI [1,1])
C0003892 (UMLS CUI [1,2])
ID.6
Item
severe concomitant disorder, e.g. other malignancy or severe heart disease
boolean
C0012634 (UMLS CUI [1])
ID.7
Item
transformation to plasma cell leukemia or aggressive lymphoma
boolean
C0023484 (UMLS CUI [1,1])
C0024299 (UMLS CUI [1,2])
C0580822 (UMLS CUI [1,3])
ID.8
Item
frequent visits for bortezomib injections not feasible
boolean
C4276228 (UMLS CUI [1])
ID.9
Item
anticipated non-adherence to study protocol
boolean
C1321605 (UMLS CUI [1])
ID.10
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
ID.11
Item
anticipated non-adherence to rules for prevention of pregnancy
boolean
C1321605 (UMLS CUI [1,1])
C0032961 (UMLS CUI [1,2])
ID.12
Item
severe thrombocytopenia (thrombocyte count less than 25000/microliter)
boolean
C0040034 (UMLS CUI [1])

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