ID

16455

Descripción

Pharmacogenetics of Anastrozole in Postmenopausal Women With Estrogen Receptor-Positive and/or Progesterone Receptor-Positive Stage I, Stage II, or Stage III Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00283608

Link

https://clinicaltrials.gov/show/NCT00283608

Palabras clave

  1. 17/7/16 17/7/16 -
Subido en

17 de julio de 2016

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY 4.0

Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Eligibility Breast Cancer NCT00283608

Eligibility Breast Cancer NCT00283608

Criteria
Descripción

Criteria

diagnosis of breast cancer
Descripción

Breast cancer

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0678222
stage i, ii, or iii disease
Descripción

Tumor stage

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1300072
resected disease
Descripción

Resection

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0728940
planning to undergo treatment with anastrozole at the clinically approved dose of 1 mg/day or mayo clinic cancer center rochester patient who will be enrolled on or has been enrolled on can-ncic-ma27 and has not started taking the study medication (anastrozole or exemestane)
Descripción

Planned treatment with anastrozole

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3641097
UMLS CUI [1,2]
C0290883
hormone receptor status:
Descripción

hormone receptor status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0019929
estrogen receptor-positive and/or progesterone receptor-positive primary tumor
Descripción

estrogen receptor-positive and/or progesterone receptor-positive primary tumor

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2919271
UMLS CUI [2]
C2919590
patient characteristics:
Descripción

Patient characteristics

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0815172
female
Descripción

Gender

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0079399
postmenopausal
Descripción

Menopausal status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0025320
able to complete questionnaires alone or with assistance
Descripción

Questionnaire

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0034394
prior concurrent therapy:
Descripción

Prior concurrent therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0009429
more than 6 months since prior endocrine therapy, except tamoxifen
Descripción

prior endocrine therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0279025
no other prior aromatase inhibitors (e.g., letrozole or exemestane)
Descripción

Aromatase inhibitors

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0593802
no prior ovarian function suppression with surgery or radiotherapy, ovarian ablation, or luteinizing hormone-releasing hormone analogues (e.g., goserelin) as treatment for cancer
Descripción

Ovarian suppression

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0677922

Similar models

Eligibility Breast Cancer NCT00283608

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Breast cancer
Item
diagnosis of breast cancer
boolean
C0678222 (UMLS CUI [1])
Tumor stage
Item
stage i, ii, or iii disease
boolean
C1300072 (UMLS CUI [1])
Resection
Item
resected disease
boolean
C0728940 (UMLS CUI [1])
Planned treatment with anastrozole
Item
planning to undergo treatment with anastrozole at the clinically approved dose of 1 mg/day or mayo clinic cancer center rochester patient who will be enrolled on or has been enrolled on can-ncic-ma27 and has not started taking the study medication (anastrozole or exemestane)
boolean
C3641097 (UMLS CUI [1,1])
C0290883 (UMLS CUI [1,2])
hormone receptor status
Item
hormone receptor status:
boolean
C0019929 (UMLS CUI [1])
estrogen receptor-positive and/or progesterone receptor-positive primary tumor
Item
estrogen receptor-positive and/or progesterone receptor-positive primary tumor
boolean
C2919271 (UMLS CUI [1])
C2919590 (UMLS CUI [2])
Patient characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Gender
Item
female
boolean
C0079399 (UMLS CUI [1])
Menopausal status
Item
postmenopausal
boolean
C0025320 (UMLS CUI [1])
Questionnaire
Item
able to complete questionnaires alone or with assistance
boolean
C0034394 (UMLS CUI [1])
Prior concurrent therapy
Item
prior concurrent therapy:
boolean
C0009429 (UMLS CUI [1])
prior endocrine therapy
Item
more than 6 months since prior endocrine therapy, except tamoxifen
boolean
C0279025 (UMLS CUI [1])
Aromatase inhibitors
Item
no other prior aromatase inhibitors (e.g., letrozole or exemestane)
boolean
C0593802 (UMLS CUI [1])
Ovarian suppression
Item
no prior ovarian function suppression with surgery or radiotherapy, ovarian ablation, or luteinizing hormone-releasing hormone analogues (e.g., goserelin) as treatment for cancer
boolean
C0677922 (UMLS CUI [1])

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial