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Information:
Fel:
ID
19576
Beskrivning
Breast Density, Hormone Levels, and Anticancer Drug Levels in Women With Invasive Breast Cancer Who Are Receiving Exemestane or Anastrozole; ODM derived from: https://clinicaltrials.gov/show/NCT00316836
Länk
https://clinicaltrials.gov/show/NCT00316836
Nyckelord
Versioner (2)
- 2017-01-11 2017-01-11 -
- 2021-09-20 2021-09-20 -
Uppladdad den
11 januari 2017
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00316836
Eligibility Breast Cancer NCT00316836
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00316836
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Invasive carcinoma of breast
Item
histologically confirmed invasive breast cancer
boolean
C0853879 (UMLS CUI [1])
Disease Complete excision
Item
completely resected disease
boolean
C0012634 (UMLS CUI [1,1])
C0015250 (UMLS CUI [1,2])
C0015250 (UMLS CUI [1,2])
Breast One Intact | Operation on breast | Biopsy of breast
Item
one intact, noncancerous breast with no prior breast surgery in that breast except breast biopsy
boolean
C0006141 (UMLS CUI [1,1])
C0205447 (UMLS CUI [1,2])
C0205266 (UMLS CUI [1,3])
C3714726 (UMLS CUI [2])
C0405352 (UMLS CUI [3])
C0205447 (UMLS CUI [1,2])
C0205266 (UMLS CUI [1,3])
C3714726 (UMLS CUI [2])
C0405352 (UMLS CUI [3])
Mammogram Available Breast Intact
Item
mammogram available taken within 12 months prior to enrollment that includes side- and top-down views of the intact, noncancerous breast
boolean
C0024671 (UMLS CUI [1,1])
C0470187 (UMLS CUI [1,2])
C0006141 (UMLS CUI [1,3])
C0205266 (UMLS CUI [1,4])
C0470187 (UMLS CUI [1,2])
C0006141 (UMLS CUI [1,3])
C0205266 (UMLS CUI [1,4])
Estrogen receptor positive tumor | Progesterone receptor positive tumor
Item
estrogen receptor- and/or progesterone receptor-positive tumor
boolean
C1562312 (UMLS CUI [1])
C1562928 (UMLS CUI [2])
C1562928 (UMLS CUI [2])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Gender
Item
female
boolean
C0079399 (UMLS CUI [1])
Postmenopausal state
Item
postmenopausal
boolean
C0232970 (UMLS CUI [1])
Mammogram Repeat Agreement
Item
agrees to retrieve and digitize mammograms taken prior to registration (within 12 months prior to atudy entry) and at approximately 1 and 2 years post-registration to this study
boolean
C0024671 (UMLS CUI [1,1])
C0205341 (UMLS CUI [1,2])
C0680240 (UMLS CUI [1,3])
C0205341 (UMLS CUI [1,2])
C0680240 (UMLS CUI [1,3])
Blood Bank Specimen Additional Agreement
Item
agrees to have an additional blood banking specimen drawn at the same time as pre-treatment specimens are drawn for parent protocol can-ncic-ma27
boolean
C0005770 (UMLS CUI [1,1])
C0370003 (UMLS CUI [1,2])
C1524062 (UMLS CUI [1,3])
C0680240 (UMLS CUI [1,4])
C0370003 (UMLS CUI [1,2])
C1524062 (UMLS CUI [1,3])
C0680240 (UMLS CUI [1,4])
Blood sample Agreement
Item
agrees to have blood sample taken at 12 months post-registration on this study
boolean
C0178913 (UMLS CUI [1,1])
C0680240 (UMLS CUI [1,2])
C0680240 (UMLS CUI [1,2])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
disease characteristic
Item
see disease characteristics
boolean
C0599878 (UMLS CUI [1])
Hormone replacement therapy | Contraceptives, Oral | Tamoxifen | Raloxifene | Selective Estrogen Receptor Modulators | Gonadotropin-Releasing Hormone Analog
Item
more than 6 months since prior hormone replacement therapy, oral contraceptives, tamoxifen, raloxifene, other selective estrogen-receptor modulators, or gonadotropin releasing-hormone analogues before pre-registration mammogram
boolean
C0282402 (UMLS CUI [1])
C0009905 (UMLS CUI [2])
C0039286 (UMLS CUI [3])
C0244404 (UMLS CUI [4])
C0732611 (UMLS CUI [5])
C1268900 (UMLS CUI [6])
C0009905 (UMLS CUI [2])
C0039286 (UMLS CUI [3])
C0244404 (UMLS CUI [4])
C0732611 (UMLS CUI [5])
C1268900 (UMLS CUI [6])