ID

13035

Beskrivning

Effectiveness of Combination of Arimidex and Nolvadex in Adjuvant Therapy of Breast Carcinoma in Postmenopausal Women.; ODM derived from: https://clinicaltrials.gov/show/NCT00287534

Länk

https://clinicaltrials.gov/show/NCT00287534

Nyckelord

  1. 2016-01-12 2016-01-12 -
Uppladdad den

12 januari 2016

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00287534

Eligibility Breast Cancer NCT00287534

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
signed informed consent,
Beskrivning

informed consent,

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
post-menopausal women ≤75 years,
Beskrivning

Age, gender, postmenopausal

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C0079399
UMLS CUI [3]
C0232970
histologically confirmed invasive breast carcinoma (no distant metastases),
Beskrivning

invasive breast carcinoma, metastases

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0205281
UMLS CUI [2]
C0027627
positive hormone receptor status,
Beskrivning

hormone receptor status

Datatyp

boolean

Alias
UMLS CUI [1]
C0019929
continuous 2-year adjuvant tamoxifen therapy 20 mg/30 mg with 4 weeks after primary surgery
Beskrivning

tamoxifen

Datatyp

boolean

Alias
UMLS CUI [1]
C0039286
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
menopause status maintained by medication,
Beskrivning

menopause status

Datatyp

boolean

Alias
UMLS CUI [1]
C0455962
pre-operative chemotherapy or hormone therapy or radiation therapy,
Beskrivning

pre-operative therapy

Datatyp

boolean

Alias
UMLS CUI [1]
C0600558
UMLS CUI [2]
C0392920
UMLS CUI [3]
C0279025
UMLS CUI [4]
C1522449
relapse or second carcinoma or previous cancerous disease,
Beskrivning

relapse and other malignant neoplasms

Datatyp

boolean

Alias
UMLS CUI [1]
C0277556
UMLS CUI [2]
C0006826
breast carcinoma in situ,
Beskrivning

breast carcinoma in situ

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0007099
simultaneous carcinoma of the opposite side or secondary breast,
Beskrivning

simultaneous carcinoma of the opposite side

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0441988
10 or more tumour-infiltrated lymph nodes.
Beskrivning

lymph nodes

Datatyp

boolean

Alias
UMLS CUI [1]
C0024204
serious accompanying diseases
Beskrivning

comorbidities

Datatyp

boolean

Alias
UMLS CUI [1]
C0009488

Similar models

Eligibility Breast Cancer NCT00287534

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
informed consent,
Item
signed informed consent,
boolean
C0021430 (UMLS CUI [1])
Age, gender, postmenopausal
Item
post-menopausal women ≤75 years,
boolean
C0001779 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
C0232970 (UMLS CUI [3])
invasive breast carcinoma, metastases
Item
histologically confirmed invasive breast carcinoma (no distant metastases),
boolean
C0678222 (UMLS CUI [1,1])
C0205281 (UMLS CUI [1,2])
C0027627 (UMLS CUI [2])
hormone receptor status
Item
positive hormone receptor status,
boolean
C0019929 (UMLS CUI [1])
tamoxifen
Item
continuous 2-year adjuvant tamoxifen therapy 20 mg/30 mg with 4 weeks after primary surgery
boolean
C0039286 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
menopause status
Item
menopause status maintained by medication,
boolean
C0455962 (UMLS CUI [1])
pre-operative therapy
Item
pre-operative chemotherapy or hormone therapy or radiation therapy,
boolean
C0600558 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
C0279025 (UMLS CUI [3])
C1522449 (UMLS CUI [4])
relapse and other malignant neoplasms
Item
relapse or second carcinoma or previous cancerous disease,
boolean
C0277556 (UMLS CUI [1])
C0006826 (UMLS CUI [2])
breast carcinoma in situ
Item
breast carcinoma in situ,
boolean
C0678222 (UMLS CUI [1,1])
C0007099 (UMLS CUI [1,2])
simultaneous carcinoma of the opposite side
Item
simultaneous carcinoma of the opposite side or secondary breast,
boolean
C0678222 (UMLS CUI [1,1])
C0441988 (UMLS CUI [1,2])
lymph nodes
Item
10 or more tumour-infiltrated lymph nodes.
boolean
C0024204 (UMLS CUI [1])
comorbidities
Item
serious accompanying diseases
boolean
C0009488 (UMLS CUI [1])

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