ID

14828

Beschrijving

Randomized Phase III Study Of Exemestane (Aromasin) For 5 Years Versus Tamoxifen for 2.5 to 3 Years Followed By Exemestane; ODM derived from: https://clinicaltrials.gov/show/NCT00036270

Link

https://clinicaltrials.gov/show/NCT00036270

Trefwoorden

  1. 01-05-16 01-05-16 -
Geüploaded op

1 mei 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Breast Neoplasms NCT00036270

Eligibility Breast Neoplasms NCT00036270

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically/cytologically confirmed adenocarcinoma of the breast, followed by adequate surgical resection and/or radiotherapy, and/or adjuvant chemotherapy, if indicated.
Beschrijving

ID.1

Datatype

boolean

Alias
UMLS CUI [1,1]
C0858252
UMLS CUI [1,2]
C0679557
UMLS CUI [2]
C0728940
UMLS CUI [3]
C1522449
UMLS CUI [4]
C0392920
stage t1-3 n0-2 mo, any tnm stage bc for whom adjuvant hormonal therapy is being considered.
Beschrijving

ID.2

Datatype

boolean

Alias
UMLS CUI [1]
C1515169
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
those patients not deemed to have had potentially curative primary surgical treatment or one of the following criteria:
Beschrijving

ID.3

Datatype

boolean

Alias
UMLS CUI [1,1]
C0038894
UMLS CUI [1,2]
C1276305
inflammatory breast cancer
Beschrijving

ID.4

Datatype

boolean

Alias
UMLS CUI [1]
C0278601
histologically positive supraclavicular nodes
Beschrijving

ID.5

Datatype

boolean

Alias
UMLS CUI [1,1]
C0229730
UMLS CUI [1,2]
C0019638
ulceration/infiltration of local skin metastasis
Beschrijving

ID.6

Datatype

boolean

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C1123023
UMLS CUI [1,3]
C0041582
UMLS CUI [1,4]
C0332448
neoadjuvant chemotherapy
Beschrijving

ID.7

Datatype

boolean

Alias
UMLS CUI [1,1]
C0600558
UMLS CUI [1,2]
C3665472
ductal carcinoma in situ (dcis) or lobular carcinoma in situ (lcis) without invasion
Beschrijving

ID.8

Datatype

boolean

Alias
UMLS CUI [1]
C0007124
UMLS CUI [2]
C0279563
er and pr negative primary tumor or er/pr unknown status.
Beschrijving

ID.9

Datatype

boolean

Alias
UMLS CUI [1]
C2919271
UMLS CUI [2]
C2919590

Similar models

Eligibility Breast Neoplasms NCT00036270

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
histologically/cytologically confirmed adenocarcinoma of the breast, followed by adequate surgical resection and/or radiotherapy, and/or adjuvant chemotherapy, if indicated.
boolean
C0858252 (UMLS CUI [1,1])
C0679557 (UMLS CUI [1,2])
C0728940 (UMLS CUI [2])
C1522449 (UMLS CUI [3])
C0392920 (UMLS CUI [4])
ID.2
Item
stage t1-3 n0-2 mo, any tnm stage bc for whom adjuvant hormonal therapy is being considered.
boolean
C1515169 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
ID.3
Item
those patients not deemed to have had potentially curative primary surgical treatment or one of the following criteria:
boolean
C0038894 (UMLS CUI [1,1])
C1276305 (UMLS CUI [1,2])
ID.4
Item
inflammatory breast cancer
boolean
C0278601 (UMLS CUI [1])
ID.5
Item
histologically positive supraclavicular nodes
boolean
C0229730 (UMLS CUI [1,1])
C0019638 (UMLS CUI [1,2])
ID.6
Item
ulceration/infiltration of local skin metastasis
boolean
C0027627 (UMLS CUI [1,1])
C1123023 (UMLS CUI [1,2])
C0041582 (UMLS CUI [1,3])
C0332448 (UMLS CUI [1,4])
ID.7
Item
neoadjuvant chemotherapy
boolean
C0600558 (UMLS CUI [1,1])
C3665472 (UMLS CUI [1,2])
ID.8
Item
ductal carcinoma in situ (dcis) or lobular carcinoma in situ (lcis) without invasion
boolean
C0007124 (UMLS CUI [1])
C0279563 (UMLS CUI [2])
ID.9
Item
er and pr negative primary tumor or er/pr unknown status.
boolean
C2919271 (UMLS CUI [1])
C2919590 (UMLS CUI [2])

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