ID

26829

Descripción

Study of Breast Tissue in Women Not Previously Diagnosed With Breast Cancer Who Are Undergoing Fine Needle Aspiration; ODM derived from: https://clinicaltrials.gov/show/NCT00896636

Link

https://clinicaltrials.gov/show/NCT00896636

Palabras clave

Versiones (1)
  1. 25/10/17 25/10/17 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

25 de octubre de 2017

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00896636

Inglés

Eligibility Breast Cancer NCT00896636

1 formularios  
Criteria
Descripción

Criteria

women meeting one of the following requirements:
Descripción

Gender

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0079399
regularly cycling premenopausal women under 45 years of age
Descripción

Menstrual cycles regular | Premenopausal state | Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2229012
UMLS CUI [2]
C0232969
UMLS CUI [3]
C0001779
perimenopausal women 45-55 years of age who have had ≥ two periods in the past 6 months
Descripción

Perimenopausal state | Age | Periods Quantity

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3839366
UMLS CUI [2]
C0001779
UMLS CUI [3,1]
C0025344
UMLS CUI [3,2]
C1265611
postmenopausal women under 60 years of age (no menstrual period for 12 months and follicle-stimulating hormone (fsh) levels > 25 iu/dl)
Descripción

Postmenopausal state | Age | Periods Absent | FSH measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0232970
UMLS CUI [2]
C0001779
UMLS CUI [3,1]
C0025344
UMLS CUI [3,2]
C0332197
UMLS CUI [4]
C0202022
no history of breast cancer diagnosis or prior treatment for breast cancer
Descripción

Exclusion Criteria | Breast Carcinoma | Prior Therapy Breast Carcinoma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0680251
UMLS CUI [2]
C0678222
UMLS CUI [3,1]
C1514463
UMLS CUI [3,2]
C0678222
negative breast evaluation within the past 3 months
Descripción

Breast Evaluation Negative

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0006141
UMLS CUI [1,2]
C1261322
UMLS CUI [1,3]
C1513916
patient characteristics:
Descripción

Client Characteristics

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0815172
see disease characteristics
Descripción

ID.8

Tipo de datos

boolean

prior concurrent therapy:
Descripción

Therapeutic procedure

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0087111
no concurrent oral contraceptives
Descripción

Oral Contraceptives Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0009905
UMLS CUI [1,2]
C0332197
at least 2 weeks since prior aspirin, non-steroidal anti-inflammatory drugs, and vitamin e
Descripción

Week Quantity Since Intake | Aspirin | Anti-Inflammatory Agents, Non-Steroidal | Vitamin E

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0439230
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C1711239
UMLS CUI [1,4]
C1512806
UMLS CUI [2]
C0004057
UMLS CUI [3]
C0003211
UMLS CUI [4]
C0042874
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Similar models

Eligibility Breast Cancer NCT00896636

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Gender
Item
women meeting one of the following requirements:
boolean
C0079399 (UMLS CUI [1])
Menstrual cycles regular | Premenopausal state | Age
Item
regularly cycling premenopausal women under 45 years of age
boolean
C2229012 (UMLS CUI [1])
C0232969 (UMLS CUI [2])
C0001779 (UMLS CUI [3])
Perimenopausal state | Age | Periods Quantity
Item
perimenopausal women 45-55 years of age who have had ≥ two periods in the past 6 months
boolean
C3839366 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0025344 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
Postmenopausal state | Age | Periods Absent | FSH measurement
Item
postmenopausal women under 60 years of age (no menstrual period for 12 months and follicle-stimulating hormone (fsh) levels > 25 iu/dl)
boolean
C0232970 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0025344 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
C0202022 (UMLS CUI [4])
Exclusion Criteria | Breast Carcinoma | Prior Therapy Breast Carcinoma
Item
no history of breast cancer diagnosis or prior treatment for breast cancer
boolean
C0680251 (UMLS CUI [1])
C0678222 (UMLS CUI [2])
C1514463 (UMLS CUI [3,1])
C0678222 (UMLS CUI [3,2])
Breast Evaluation Negative
Item
negative breast evaluation within the past 3 months
boolean
C0006141 (UMLS CUI [1,1])
C1261322 (UMLS CUI [1,2])
C1513916 (UMLS CUI [1,3])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
ID.8
Item
see disease characteristics
boolean
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
Oral Contraceptives Absent
Item
no concurrent oral contraceptives
boolean
C0009905 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Week Quantity Since Intake | Aspirin | Anti-Inflammatory Agents, Non-Steroidal | Vitamin E
Item
at least 2 weeks since prior aspirin, non-steroidal anti-inflammatory drugs, and vitamin e
boolean
C0439230 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C1711239 (UMLS CUI [1,3])
C1512806 (UMLS CUI [1,4])
C0004057 (UMLS CUI [2])
C0003211 (UMLS CUI [3])
C0042874 (UMLS CUI [4])
Volver a la parte superior de la página 

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