Informatie:
Fout:
ID
26829
Beschrijving
Study of Breast Tissue in Women Not Previously Diagnosed With Breast Cancer Who Are Undergoing Fine Needle Aspiration; ODM derived from: https://clinicaltrials.gov/show/NCT00896636
Link
https://clinicaltrials.gov/show/NCT00896636
Trefwoorden
Versies (1)
- 25-10-17 25-10-17 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
25 oktober 2017
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00896636
Eligibility Breast Cancer NCT00896636
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00896636
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Gender
Item
women meeting one of the following requirements:
boolean
C0079399 (UMLS CUI [1])
Menstrual cycles regular | Premenopausal state | Age
Item
regularly cycling premenopausal women under 45 years of age
boolean
C2229012 (UMLS CUI [1])
C0232969 (UMLS CUI [2])
C0001779 (UMLS CUI [3])
C0232969 (UMLS CUI [2])
C0001779 (UMLS CUI [3])
Perimenopausal state | Age | Periods Quantity
Item
perimenopausal women 45-55 years of age who have had ≥ two periods in the past 6 months
boolean
C3839366 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0025344 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
C0001779 (UMLS CUI [2])
C0025344 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
Postmenopausal state | Age | Periods Absent | FSH measurement
Item
postmenopausal women under 60 years of age (no menstrual period for 12 months and follicle-stimulating hormone (fsh) levels > 25 iu/dl)
boolean
C0232970 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0025344 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
C0202022 (UMLS CUI [4])
C0001779 (UMLS CUI [2])
C0025344 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
C0202022 (UMLS CUI [4])
Exclusion Criteria | Breast Carcinoma | Prior Therapy Breast Carcinoma
Item
no history of breast cancer diagnosis or prior treatment for breast cancer
boolean
C0680251 (UMLS CUI [1])
C0678222 (UMLS CUI [2])
C1514463 (UMLS CUI [3,1])
C0678222 (UMLS CUI [3,2])
C0678222 (UMLS CUI [2])
C1514463 (UMLS CUI [3,1])
C0678222 (UMLS CUI [3,2])
Breast Evaluation Negative
Item
negative breast evaluation within the past 3 months
boolean
C0006141 (UMLS CUI [1,1])
C1261322 (UMLS CUI [1,2])
C1513916 (UMLS CUI [1,3])
C1261322 (UMLS CUI [1,2])
C1513916 (UMLS CUI [1,3])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
ID.8
Item
see disease characteristics
boolean
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
Oral Contraceptives Absent
Item
no concurrent oral contraceptives
boolean
C0009905 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,2])
Week Quantity Since Intake | Aspirin | Anti-Inflammatory Agents, Non-Steroidal | Vitamin E
Item
at least 2 weeks since prior aspirin, non-steroidal anti-inflammatory drugs, and vitamin e
boolean
C0439230 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C1711239 (UMLS CUI [1,3])
C1512806 (UMLS CUI [1,4])
C0004057 (UMLS CUI [2])
C0003211 (UMLS CUI [3])
C0042874 (UMLS CUI [4])
C1265611 (UMLS CUI [1,2])
C1711239 (UMLS CUI [1,3])
C1512806 (UMLS CUI [1,4])
C0004057 (UMLS CUI [2])
C0003211 (UMLS CUI [3])
C0042874 (UMLS CUI [4])