ID

19576

Description

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

Lien

https://clinicaltrials.gov/show/NCT00316836

Mots-clés

Versions (2)
  1. 11/01/2017 11/01/2017 -
  2. 20/09/2021 20/09/2021 -
Téléchargé le

11 janvier 2017

DOI

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Licence

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00316836

Anglais

Eligibility Breast Cancer NCT00316836

1 Formulaires  
Criteria
Description

Criteria

histologically confirmed invasive breast cancer
Description

Invasive carcinoma of breast

Type de données

boolean

Alias
UMLS CUI [1]
C0853879
completely resected disease
Description

Disease Complete excision

Type de données

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0015250
one intact, noncancerous breast with no prior breast surgery in that breast except breast biopsy
Description

Breast One Intact | Operation on breast | Biopsy of breast

Type de données

boolean

Alias
UMLS CUI [1,1]
C0006141
UMLS CUI [1,2]
C0205447
UMLS CUI [1,3]
C0205266
UMLS CUI [2]
C3714726
UMLS CUI [3]
C0405352
mammogram available taken within 12 months prior to enrollment that includes side- and top-down views of the intact, noncancerous breast
Description

Mammogram Available Breast Intact

Type de données

boolean

Alias
UMLS CUI [1,1]
C0024671
UMLS CUI [1,2]
C0470187
UMLS CUI [1,3]
C0006141
UMLS CUI [1,4]
C0205266
estrogen receptor- and/or progesterone receptor-positive tumor
Description

Estrogen receptor positive tumor | Progesterone receptor positive tumor

Type de données

boolean

Alias
UMLS CUI [1]
C1562312
UMLS CUI [2]
C1562928
patient characteristics:
Description

Client Characteristics

Type de données

boolean

Alias
UMLS CUI [1]
C0815172
female
Description

Gender

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
postmenopausal
Description

Postmenopausal state

Type de données

boolean

Alias
UMLS CUI [1]
C0232970
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
Description

Mammogram Repeat Agreement

Type de données

boolean

Alias
UMLS CUI [1,1]
C0024671
UMLS CUI [1,2]
C0205341
UMLS CUI [1,3]
C0680240
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
Description

Blood Bank Specimen Additional Agreement

Type de données

boolean

Alias
UMLS CUI [1,1]
C0005770
UMLS CUI [1,2]
C0370003
UMLS CUI [1,3]
C1524062
UMLS CUI [1,4]
C0680240
agrees to have blood sample taken at 12 months post-registration on this study
Description

Blood sample Agreement

Type de données

boolean

Alias
UMLS CUI [1,1]
C0178913
UMLS CUI [1,2]
C0680240
prior concurrent therapy:
Description

Therapeutic procedure

Type de données

boolean

Alias
UMLS CUI [1]
C0087111
see disease characteristics
Description

disease characteristic

Type de données

boolean

Alias
UMLS CUI [1]
C0599878
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
Description

Hormone replacement therapy | Contraceptives, Oral | Tamoxifen | Raloxifene | Selective Estrogen Receptor Modulators | Gonadotropin-Releasing Hormone Analog

Type de données

boolean

Alias
UMLS CUI [1]
C0282402
UMLS CUI [2]
C0009905
UMLS CUI [3]
C0039286
UMLS CUI [4]
C0244404
UMLS CUI [5]
C0732611
UMLS CUI [6]
C1268900
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Similar models

Eligibility Breast Cancer NCT00316836

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
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])
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])
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])
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])
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])
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])
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])
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])
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