ID

27271

Description

Breast Cancer Detection: Comparison of Breast Tomosynthesis and Conventional Mammography; ODM derived from: https://clinicaltrials.gov/show/NCT01669148

Link

https://clinicaltrials.gov/show/NCT01669148

Keywords

  1. 11/6/17 11/6/17 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

November 6, 2017

DOI

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License

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT01669148

Eligibility Breast Cancer NCT01669148

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
female
Description

Gender

Data type

boolean

Alias
UMLS CUI [1]
C0079399
any ethnic origin
Description

Ethnicity Any

Data type

boolean

Alias
UMLS CUI [1,1]
C0015031
UMLS CUI [1,2]
C1552551
no contraindication for routine bilateral mammography
Description

Medical contraindication Absent Bilateral mammography

Data type

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0332197
UMLS CUI [1,3]
C0203027
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
potential subjects with any of the following will not be enrolled in the study:
Description

Criteria Enrollment Excluded

Data type

boolean

Alias
UMLS CUI [1,1]
C0243161
UMLS CUI [1,2]
C1516879
UMLS CUI [1,3]
C2828389
any contraindications to mammographic screening, including, but not limited to:
Description

Medical contraindication Mammography

Data type

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0024671
significant existing breast trauma
Description

BREAST INJURY TRAUMA

Data type

boolean

Alias
UMLS CUI [1]
C0741715
under the age of 30 at the time of consent
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
breast implants
Description

Breast implants

Data type

boolean

Alias
UMLS CUI [1]
C0179412
prior surgeries
Description

Operative Surgical Procedures

Data type

boolean

Alias
UMLS CUI [1]
C0543467
unable to understand and execute written informed consent
Description

Informed Consent Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
pregnant
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
lactating
Description

Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0006147

Similar models

Eligibility Breast Cancer NCT01669148

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Gender
Item
female
boolean
C0079399 (UMLS CUI [1])
Ethnicity Any
Item
any ethnic origin
boolean
C0015031 (UMLS CUI [1,1])
C1552551 (UMLS CUI [1,2])
Medical contraindication Absent Bilateral mammography
Item
no contraindication for routine bilateral mammography
boolean
C1301624 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0203027 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Criteria Enrollment Excluded
Item
potential subjects with any of the following will not be enrolled in the study:
boolean
C0243161 (UMLS CUI [1,1])
C1516879 (UMLS CUI [1,2])
C2828389 (UMLS CUI [1,3])
Medical contraindication Mammography
Item
any contraindications to mammographic screening, including, but not limited to:
boolean
C1301624 (UMLS CUI [1,1])
C0024671 (UMLS CUI [1,2])
BREAST INJURY TRAUMA
Item
significant existing breast trauma
boolean
C0741715 (UMLS CUI [1])
Age
Item
under the age of 30 at the time of consent
boolean
C0001779 (UMLS CUI [1])
Breast implants
Item
breast implants
boolean
C0179412 (UMLS CUI [1])
Operative Surgical Procedures
Item
prior surgeries
boolean
C0543467 (UMLS CUI [1])
Informed Consent Unable
Item
unable to understand and execute written informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Pregnancy
Item
pregnant
boolean
C0032961 (UMLS CUI [1])
Breast Feeding
Item
lactating
boolean
C0006147 (UMLS CUI [1])

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