ID

26829

Description

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

Keywords

Versions (1)
  1. 10/25/17 10/25/17 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

October 25, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00896636

English

Eligibility Breast Cancer NCT00896636

1 forms  
Criteria
Description

Criteria

women meeting one of the following requirements:
Description

Gender

Data type

boolean

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

Menstrual cycles regular | Premenopausal state | Age

Data type

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
Description

Perimenopausal state | Age | Periods Quantity

Data type

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)
Description

Postmenopausal state | Age | Periods Absent | FSH measurement

Data type

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
Description

Exclusion Criteria | Breast Carcinoma | Prior Therapy Breast Carcinoma

Data type

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
Description

Breast Evaluation Negative

Data type

boolean

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

Client Characteristics

Data type

boolean

Alias
UMLS CUI [1]
C0815172
see disease characteristics
Description

ID.8

Data type

boolean

prior concurrent therapy:
Description

Therapeutic procedure

Data type

boolean

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

Oral Contraceptives Absent

Data type

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
Description

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

Data type

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 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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])
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