Eligibility Breast Cancer NCT00584753

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
normal adult volunteers
Description

Normal Volunteers | Adult

Data type

boolean

Alias
UMLS CUI [1]
C3661466
UMLS CUI [2]
C0001675
female, at least 18 years of age
Description

Gender | Age

Data type

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
ability to lie motionless for up to 20 minutes
Description

Able to lie down Quiet Minute Quantity

Data type

boolean

Alias
UMLS CUI [1,1]
C0560841
UMLS CUI [1,2]
C0439654
UMLS CUI [1,3]
C0439232
UMLS CUI [1,4]
C1265611
patient volunteers
Description

Clinical trial participant

Data type

boolean

Alias
UMLS CUI [1]
C1997894
female, at least 18 years of age
Description

Gender | Age

Data type

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
diagnostic findings from prior mammography highly suggestive of invasive breast carcinoma (bi-rads category 5)
Description

Mammography Suggestive of Invasive carcinoma of breast BI-RADS

Data type

boolean

Alias
UMLS CUI [1,1]
C0024671
UMLS CUI [1,2]
C0332299
UMLS CUI [1,3]
C0853879
UMLS CUI [1,4]
C1511314
not pregnant or breast-feeding
Description

Pregnancy Absent | Breast Feeding Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0006147
UMLS CUI [2,2]
C0332197
ability to lie motionless for up to 20 minutes
Description

Able to lie down Quiet Minute Quantity

Data type

boolean

Alias
UMLS CUI [1,1]
C0560841
UMLS CUI [1,2]
C0439654
UMLS CUI [1,3]
C0439232
UMLS CUI [1,4]
C1265611
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
normal adult volunteers
Description

Normal Volunteers | Adult

Data type

boolean

Alias
UMLS CUI [1]
C3661466
UMLS CUI [2]
C0001675
inability to understand the risks and benefits of the study
Description

Study Protocol Comprehension Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C2348563
UMLS CUI [1,2]
C0162340
UMLS CUI [1,3]
C1299582
patient volunteers
Description

Clinical trial participant

Data type

boolean

Alias
UMLS CUI [1]
C1997894
recent breast biopsy
Description

Biopsy of breast

Data type

boolean

Alias
UMLS CUI [1]
C0405352
diagnostic findings from prior mammography highly suggestive of noninvasive ductal or lobular carcinoma
Description

Mammography Suggestive of Noninvasive ductal carcinoma | Mammography Suggestive of Lobular Carcinoma

Data type

boolean

Alias
UMLS CUI [1,1]
C0024671
UMLS CUI [1,2]
C0332299
UMLS CUI [1,3]
C0861353
UMLS CUI [2,1]
C0024671
UMLS CUI [2,2]
C0332299
UMLS CUI [2,3]
C0206692
uncontrolled diabetes
Description

Diabetic - poor control

Data type

boolean

Alias
UMLS CUI [1]
C0421258
diabetic and blood sugar level > 200 mg/dl
Description

Blood glucose measurement Diabetic | Blood glucose measurement

Data type

boolean

Alias
UMLS CUI [1,1]
C0392201
UMLS CUI [1,2]
C0241863
UMLS CUI [2]
C0392201
positive urine pregnancy test or currently breast-feeding
Description

Urine pregnancy test positive | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0430059
UMLS CUI [2]
C0006147
inability to understand the risks and benefits of the study
Description

Study Protocol Comprehension Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C2348563
UMLS CUI [1,2]
C0162340
UMLS CUI [1,3]
C1299582

Similar models

Eligibility Breast Cancer NCT00584753

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Normal Volunteers | Adult
Item
normal adult volunteers
boolean
C3661466 (UMLS CUI [1])
C0001675 (UMLS CUI [2])
Gender | Age
Item
female, at least 18 years of age
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Able to lie down Quiet Minute Quantity
Item
ability to lie motionless for up to 20 minutes
boolean
C0560841 (UMLS CUI [1,1])
C0439654 (UMLS CUI [1,2])
C0439232 (UMLS CUI [1,3])
C1265611 (UMLS CUI [1,4])
Clinical trial participant
Item
patient volunteers
boolean
C1997894 (UMLS CUI [1])
Gender | Age
Item
female, at least 18 years of age
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Mammography Suggestive of Invasive carcinoma of breast BI-RADS
Item
diagnostic findings from prior mammography highly suggestive of invasive breast carcinoma (bi-rads category 5)
boolean
C0024671 (UMLS CUI [1,1])
C0332299 (UMLS CUI [1,2])
C0853879 (UMLS CUI [1,3])
C1511314 (UMLS CUI [1,4])
Pregnancy Absent | Breast Feeding Absent
Item
not pregnant or breast-feeding
boolean
C0032961 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0006147 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Able to lie down Quiet Minute Quantity
Item
ability to lie motionless for up to 20 minutes
boolean
C0560841 (UMLS CUI [1,1])
C0439654 (UMLS CUI [1,2])
C0439232 (UMLS CUI [1,3])
C1265611 (UMLS CUI [1,4])
Item Group
C0680251 (UMLS CUI)
Normal Volunteers | Adult
Item
normal adult volunteers
boolean
C3661466 (UMLS CUI [1])
C0001675 (UMLS CUI [2])
Study Protocol Comprehension Unable
Item
inability to understand the risks and benefits of the study
boolean
C2348563 (UMLS CUI [1,1])
C0162340 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
Clinical trial participant
Item
patient volunteers
boolean
C1997894 (UMLS CUI [1])
Biopsy of breast
Item
recent breast biopsy
boolean
C0405352 (UMLS CUI [1])
Mammography Suggestive of Noninvasive ductal carcinoma | Mammography Suggestive of Lobular Carcinoma
Item
diagnostic findings from prior mammography highly suggestive of noninvasive ductal or lobular carcinoma
boolean
C0024671 (UMLS CUI [1,1])
C0332299 (UMLS CUI [1,2])
C0861353 (UMLS CUI [1,3])
C0024671 (UMLS CUI [2,1])
C0332299 (UMLS CUI [2,2])
C0206692 (UMLS CUI [2,3])
Diabetic - poor control
Item
uncontrolled diabetes
boolean
C0421258 (UMLS CUI [1])
Blood glucose measurement Diabetic | Blood glucose measurement
Item
diabetic and blood sugar level > 200 mg/dl
boolean
C0392201 (UMLS CUI [1,1])
C0241863 (UMLS CUI [1,2])
C0392201 (UMLS CUI [2])
Urine pregnancy test positive | Breast Feeding
Item
positive urine pregnancy test or currently breast-feeding
boolean
C0430059 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Study Protocol Comprehension Unable
Item
inability to understand the risks and benefits of the study
boolean
C2348563 (UMLS CUI [1,1])
C0162340 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])