Informatie:
Fout:
ID
21472
Beschrijving
A Study of Bortezomib, Cyclophosphamide, and Dexamethasone in Patients With Untreated Multiple Myeloma and Planned for a High Dose Chemotherapy; ODM derived from: https://clinicaltrials.gov/show/NCT00833560
Link
https://clinicaltrials.gov/show/NCT00833560
Trefwoorden
Versies (1)
- 23-04-17 23-04-17 -
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23 april 2017
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Multiple Myeloma DRKS00003762 NCT00833560
Eligibility Multiple Myeloma NCT00833560
- StudyEvent: Eligibility
Similar models
Eligibility Multiple Myeloma NCT00833560
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Multiple Myeloma Stage
Item
cytologically or histologically diagnosed with multiple myeloma stage ii/iii
boolean
C0026764 (UMLS CUI [1,1])
C1300072 (UMLS CUI [1,2])
C1300072 (UMLS CUI [1,2])
Chemotherapy Regimen
Item
participants without preceding cytostatic (tending to retard cellular activity and multiplication) treatment (pretreatment with radiation or dexamethasone is allowed)
boolean
C0392920 (UMLS CUI [1])
Contraceptive methods
Item
agree to use one of the contraception methods as defined in the protocol
boolean
C0700589 (UMLS CUI [1])
Karnofsky Performance Status
Item
karnofsky performance status 60 percent or more
boolean
C0206065 (UMLS CUI [1])
Laboratory Test Result
Item
adequate laboratory test values
boolean
C2346633 (UMLS CUI [1])
Non-secretory multiple myeloma
Item
non-secretory multiple myeloma
boolean
C0456845 (UMLS CUI [1])
Life expectancy
Item
estimated life expectancy less than 3 months
boolean
C0023671 (UMLS CUI [1])
Prior malignancy
Item
history of cancer (except basal cell carcinoma) in the last 5 years
boolean
C2735088 (UMLS CUI [1])
Neuropathy grade
Item
peripheral neuropathy (disorder of the peripheral nerves) grade 2 or more
boolean
C0442874 (UMLS CUI [1,1])
C0441800 (UMLS CUI [1,2])
C0441800 (UMLS CUI [1,2])
HIV, HBV, HCV
Item
positive human immunodeficiency virus test and active hepatitis b and/or hepatitis c
boolean
C0019699 (UMLS CUI [1])
C0149709 (UMLS CUI [2])
C1112419 (UMLS CUI [3])
C0149709 (UMLS CUI [2])
C1112419 (UMLS CUI [3])
Gynaecological status
Item
pregnant or breast-feeding female participants
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])