ID

16347

Descripción

Protocol for Women at Increased Risk of Developing Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00291135

Link

https://clinicaltrials.gov/show/NCT00291135

Palabras clave

Versiones (1)
  1. 11/7/16 11/7/16 -
Subido en

11 de julio de 2016

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00291135

Inglés

Eligibility Breast Cancer NCT00291135

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
evidence of hyperplasia with/without atypia upon random periareolar fine needle aspiration of breast
Descripción

Random Periareolar Fine-Needle Aspiration | Evidence of Breast hyperplasia | Evidence of Atypical hyperplasia of breast

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3640066
UMLS CUI [2,1]
C0332120
UMLS CUI [2,2]
C0542028
UMLS CUI [3,1]
C0332120
UMLS CUI [3,2]
C1297929
on hormone replacement therapy
Descripción

Hormone replacement therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0282402
postmenopausal
Descripción

Postmenopausal state

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0232970
increased risk of developing breast cancer based on personal or family history
Descripción

Increased risk of breast cancer in women Due to Medical History | Increased risk of breast cancer in women Due to Family history

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2676211
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0262926
UMLS CUI [2,1]
C2676211
UMLS CUI [2,2]
C0678226
UMLS CUI [2,3]
C0241889
never have taken aromatase inhibitors or selective estrogen receptor modulators in last six months
Descripción

Aromatase Inhibitors | Selective Estrogen Receptor Modulators

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0593802
UMLS CUI [2]
C0732611
women who have a high risk of breast cancer
Descripción

Gender | Breast Carcinoma High risk

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2,1]
C0678222
UMLS CUI [2,2]
C0332167
older than 18 years
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
anticoagulants
Descripción

Anticoagulants

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0003280
marked breast tenderness
Descripción

Breast tenderness Marked

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0262397
UMLS CUI [1,2]
C1706089
pregnant or within twelve months of breast feeding/childbirth
Descripción

Pregnancy | Breast Feeding | Childbirth

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3]
C1148523
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Similar models

Eligibility Breast Cancer NCT00291135

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Random Periareolar Fine-Needle Aspiration | Evidence of Breast hyperplasia | Evidence of Atypical hyperplasia of breast
Item
evidence of hyperplasia with/without atypia upon random periareolar fine needle aspiration of breast
boolean
C3640066 (UMLS CUI [1])
C0332120 (UMLS CUI [2,1])
C0542028 (UMLS CUI [2,2])
C0332120 (UMLS CUI [3,1])
C1297929 (UMLS CUI [3,2])
Hormone replacement therapy
Item
on hormone replacement therapy
boolean
C0282402 (UMLS CUI [1])
Postmenopausal state
Item
postmenopausal
boolean
C0232970 (UMLS CUI [1])
Increased risk of breast cancer in women Due to Medical History | Increased risk of breast cancer in women Due to Family history
Item
increased risk of developing breast cancer based on personal or family history
boolean
C2676211 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0262926 (UMLS CUI [1,3])
C2676211 (UMLS CUI [2,1])
C0678226 (UMLS CUI [2,2])
C0241889 (UMLS CUI [2,3])
Aromatase Inhibitors | Selective Estrogen Receptor Modulators
Item
never have taken aromatase inhibitors or selective estrogen receptor modulators in last six months
boolean
C0593802 (UMLS CUI [1])
C0732611 (UMLS CUI [2])
Gender | Breast Carcinoma High risk
Item
women who have a high risk of breast cancer
boolean
C0079399 (UMLS CUI [1])
C0678222 (UMLS CUI [2,1])
C0332167 (UMLS CUI [2,2])
Age
Item
older than 18 years
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Anticoagulants
Item
anticoagulants
boolean
C0003280 (UMLS CUI [1])
Breast tenderness Marked
Item
marked breast tenderness
boolean
C0262397 (UMLS CUI [1,1])
C1706089 (UMLS CUI [1,2])
Pregnancy | Breast Feeding | Childbirth
Item
pregnant or within twelve months of breast feeding/childbirth
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C1148523 (UMLS CUI [3])
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