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Informatie:
Fout:
ID
14832
Beschrijving
Study of ABI-007 and Taxol in Patients With Metastatic Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00046527
Link
https://clinicaltrials.gov/show/NCT00046527
Trefwoorden
Versies (2)
- 01-05-16 01-05-16 -
- 20-09-21 20-09-21 -
Geüploaded op
1 mei 2016
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Breast Neoplasms NCT00046527
Eligibility Breast Neoplasms NCT00046527
- StudyEvent: Eligibility
Similar models
Eligibility Breast Neoplasms NCT00046527
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
ID.1
Item
female, non-pregnant, non-lactating, and, if of child-bearing potential, have a negative serum pregnancy test, and use approved contraception
boolean
C0015780 (UMLS CUI [1])
C0032961 (UMLS CUI [2])
C0006147 (UMLS CUI [3])
C0015895 (UMLS CUI [4])
C0700589 (UMLS CUI [5])
C0032961 (UMLS CUI [2])
C0006147 (UMLS CUI [3])
C0015895 (UMLS CUI [4])
C0700589 (UMLS CUI [5])
ID.2
Item
sixteen years of age or older
boolean
C0001779 (UMLS CUI [1])
ID.3
Item
histologically or cytologically confirmed breast cancer (stage iii or iv) with evidence of inoperable local recurrence or metastasis, with measurable disease
boolean
C0678222 (UMLS CUI [1,1])
C0019638 (UMLS CUI [1,2])
C1300072 (UMLS CUI [1,3])
C0205187 (UMLS CUI [2])
C1513041 (UMLS CUI [3])
C0019638 (UMLS CUI [1,2])
C1300072 (UMLS CUI [1,3])
C0205187 (UMLS CUI [2])
C1513041 (UMLS CUI [3])
ID.4
Item
if patient has received taxane therapy as an adjuvant he/she has not relapsed within one year of completing adjuvant taxane
boolean
C3541958 (UMLS CUI [1,1])
C0277556 (UMLS CUI [1,2])
C0277556 (UMLS CUI [1,2])
ID.5
Item
no other malignancy present within the past 5 years, except non-melanoma skin cancer, cervical intraepithelial neoplasia or in-situ cervical cancer
boolean
C0006826 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
ID.6
Item
suitable candidate for paclitaxel therapy
boolean
C0144576 (UMLS CUI [1,1])
C0332149 (UMLS CUI [1,2])
C0332149 (UMLS CUI [1,2])
ID.7
Item
hematology levels at baseline of: absolute neutrophil count of at least 1500 cells/mm3; platelet count of at least 100,000 cells/mm3; hemoglobin of at least 9 g/dl
boolean
C0948762 (UMLS CUI [1])
C0005821 (UMLS CUI [2])
C0019046 (UMLS CUI [3])
C0005821 (UMLS CUI [2])
C0019046 (UMLS CUI [3])
ID.8
Item
chemistry levels at baseline of: ast and alt of less than or equal to 2.5 x the upper limit of normal, if no evidence of liver metastasis; total bilirubin of less than or equal to 1.5 mg/dl; creatinine of less than or equal to 2 mg/dl; alkaline phosphatase of less than or equal to 5 x the upper limit of normal, unless there is bone metastasis but not liver metastasis
boolean
C0201899 (UMLS CUI [1])
C0201836 (UMLS CUI [2])
C1278039 (UMLS CUI [3])
C0201850 (UMLS CUI [4])
C0201976 (UMLS CUI [5])
C0201836 (UMLS CUI [2])
C1278039 (UMLS CUI [3])
C0201850 (UMLS CUI [4])
C0201976 (UMLS CUI [5])
ID.9
Item
expected survival of at least 12 weeks
boolean
C0023671 (UMLS CUI [1])
ID.10
Item
patient or his/her representative has signed an informed consent form
boolean
C0021430 (UMLS CUI [1])