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Informatie:
Fout:
ID
16423
Beschrijving
Evaluation of Patients With Breast Cancer Using DCE-MRI, MRS, and Proteomics; ODM derived from: https://clinicaltrials.gov/show/NCT00656604
Link
https://clinicaltrials.gov/show/NCT00656604
Trefwoorden
Versies (2)
- 15-07-16 15-07-16 -
- 17-09-21 17-09-21 -
Geüploaded op
15 juli 2016
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00656604
Eligibility Breast Cancer NCT00656604
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00656604
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
criteria Fulfill
Item
meets 1 of the following criteria:
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
C1550543 (UMLS CUI [1,2])
Gender | Breast Carcinoma | Excision Planned
Item
women with breast tumors planning to undergo surgical resection
boolean
C0079399 (UMLS CUI [1])
C0678222 (UMLS CUI [2])
C0728940 (UMLS CUI [3,1])
C1301732 (UMLS CUI [3,2])
C0678222 (UMLS CUI [2])
C0728940 (UMLS CUI [3,1])
C1301732 (UMLS CUI [3,2])
Healthy Volunteers | Well female adult | Breast Carcinoma
Item
healthy volunteers, including any constitutionally healthy female with no history of breast cancer
boolean
C1708335 (UMLS CUI [1])
C0686752 (UMLS CUI [2])
C0678222 (UMLS CUI [3])
C0686752 (UMLS CUI [2])
C0678222 (UMLS CUI [3])
Hormone Receptor Status Unspecified
Item
hormone receptor status not specified
boolean
C0019929 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,3])
C0449438 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,3])
patient characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Gender
Item
female
boolean
C0079399 (UMLS CUI [1])
Menopausal Status Unspecified
Item
menopausal status not specified
boolean
C1513126 (UMLS CUI [1,1])
C0205370 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
not pregnant or nursing
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Pregnancy test negative
Item
negative pregnancy test
boolean
C0427780 (UMLS CUI [1])
Fertility Contraceptive methods
Item
fertile patients must use effective contraception
boolean
C0015895 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0700589 (UMLS CUI [1,2])
Illness
Item
not acutely ill
boolean
C0221423 (UMLS CUI [1])
Foreign materials Magnetic metal Present Body
Item
no non-magnetic resonance-compatible ferromagnetic materials present in the body
boolean
C0016542 (UMLS CUI [1,1])
C0439876 (UMLS CUI [1,2])
C0150312 (UMLS CUI [1,3])
C1268086 (UMLS CUI [1,4])
C0439876 (UMLS CUI [1,2])
C0150312 (UMLS CUI [1,3])
C1268086 (UMLS CUI [1,4])
concurrent therapy
Item
prior concurrent therapy:
boolean
C0009429 (UMLS CUI [1])
Prior Chemotherapy | prior radiation therapy
Item
prior chemotherapy and/or radiotherapy allowed
boolean
C1514457 (UMLS CUI [1])
C0279134 (UMLS CUI [2])
C0279134 (UMLS CUI [2])