Eligibility Breast Cancer NCT00094133

Criteria
Description

Criteria

history of primary breast cancer
Description

Primary malignant neoplasm of breast

Data type

boolean

Alias
UMLS CUI [1]
C1299258
no evidence of detectable disease
Description

Disease Detectable Evidence

Data type

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C3830527
UMLS CUI [1,3]
C3887511
at least 14 hot flashes per week for ≥ 1 month by self-reporting
Description

Hot flashes Quantity Weekly

Data type

boolean

Alias
UMLS CUI [1,1]
C0600142
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C0332174
hormone receptor status not specified
Description

Hormone Receptor Status Unspecified

Data type

boolean

Alias
UMLS CUI [1,1]
C0019929
UMLS CUI [1,2]
C0449438
UMLS CUI [1,3]
C0205370
patient characteristics:
Description

Client Characteristics

Data type

boolean

Alias
UMLS CUI [1]
C0815172
female
Description

Gender

Data type

boolean

Alias
UMLS CUI [1]
C0079399
life expectancy > 6 months
Description

Life Expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
menopausal status not specified
Description

Menopausal Status Unspecified

Data type

boolean

Alias
UMLS CUI [1,1]
C1513126
UMLS CUI [1,2]
C0205370
outpatient status
Description

Outpatient

Data type

boolean

Alias
UMLS CUI [1]
C0029921
no medical or psychiatric condition that would preclude study participation
Description

Medical condition Study Subject Participation Status Exclusion | Mental disorder Study Subject Participation Status Exclusion

Data type

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C2348568
UMLS CUI [1,3]
C2828389
UMLS CUI [2,1]
C0004936
UMLS CUI [2,2]
C2348568
UMLS CUI [2,3]
C2828389
prior concurrent therapy:
Description

Therapeutic procedure

Data type

boolean

Alias
UMLS CUI [1]
C0087111
concurrent antihormonal agents for breast cancer (e.g., tamoxifen or raloxifene) allowed provided the patient has been on them for ≥ 1 month
Description

Hormone Antagonists Breast Carcinoma | Tamoxifen | Raloxifene

Data type

boolean

Alias
UMLS CUI [1,1]
C0019927
UMLS CUI [1,2]
C0678222
UMLS CUI [2]
C0039286
UMLS CUI [3]
C0244404
no other concurrent hormonal therapy
Description

Hormone Therapy

Data type

boolean

Alias
UMLS CUI [1]
C0279025
no other putative therapies for hot flashes ≥ 1 month prior to study entry
Description

Therapeutic procedure Suspected Hot flashes

Data type

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0750491
UMLS CUI [1,3]
C0600142
concurrent vitamin e allowed
Description

Vitamin E

Data type

boolean

Alias
UMLS CUI [1]
C0042874
no other concurrent treatment for hot flashes
Description

Therapeutic procedure Hot flashes

Data type

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0600142
no concurrent cytotoxic chemotherapy
Description

Cytotoxic Chemotherapy

Data type

boolean

Alias
UMLS CUI [1]
C0677881
not concurrently using hypnosis for any reason
Description

Hypnosis reason for

Data type

boolean

Alias
UMLS CUI [1,1]
C3888013
UMLS CUI [1,2]
C0392360

Similar models

Eligibility Breast Cancer NCT00094133

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Primary malignant neoplasm of breast
Item
history of primary breast cancer
boolean
C1299258 (UMLS CUI [1])
Disease Detectable Evidence
Item
no evidence of detectable disease
boolean
C0012634 (UMLS CUI [1,1])
C3830527 (UMLS CUI [1,2])
C3887511 (UMLS CUI [1,3])
Hot flashes Quantity Weekly
Item
at least 14 hot flashes per week for ≥ 1 month by self-reporting
boolean
C0600142 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0332174 (UMLS CUI [1,3])
Hormone Receptor Status Unspecified
Item
hormone receptor status not specified
boolean
C0019929 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,3])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Gender
Item
female
boolean
C0079399 (UMLS CUI [1])
Life Expectancy
Item
life expectancy > 6 months
boolean
C0023671 (UMLS CUI [1])
Menopausal Status Unspecified
Item
menopausal status not specified
boolean
C1513126 (UMLS CUI [1,1])
C0205370 (UMLS CUI [1,2])
Outpatient
Item
outpatient status
boolean
C0029921 (UMLS CUI [1])
Medical condition Study Subject Participation Status Exclusion | Mental disorder Study Subject Participation Status Exclusion
Item
no medical or psychiatric condition that would preclude study participation
boolean
C3843040 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C2828389 (UMLS CUI [1,3])
C0004936 (UMLS CUI [2,1])
C2348568 (UMLS CUI [2,2])
C2828389 (UMLS CUI [2,3])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
Hormone Antagonists Breast Carcinoma | Tamoxifen | Raloxifene
Item
concurrent antihormonal agents for breast cancer (e.g., tamoxifen or raloxifene) allowed provided the patient has been on them for ≥ 1 month
boolean
C0019927 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
C0039286 (UMLS CUI [2])
C0244404 (UMLS CUI [3])
Hormone Therapy
Item
no other concurrent hormonal therapy
boolean
C0279025 (UMLS CUI [1])
Therapeutic procedure Suspected Hot flashes
Item
no other putative therapies for hot flashes ≥ 1 month prior to study entry
boolean
C0087111 (UMLS CUI [1,1])
C0750491 (UMLS CUI [1,2])
C0600142 (UMLS CUI [1,3])
Vitamin E
Item
concurrent vitamin e allowed
boolean
C0042874 (UMLS CUI [1])
Therapeutic procedure Hot flashes
Item
no other concurrent treatment for hot flashes
boolean
C0087111 (UMLS CUI [1,1])
C0600142 (UMLS CUI [1,2])
Cytotoxic Chemotherapy
Item
no concurrent cytotoxic chemotherapy
boolean
C0677881 (UMLS CUI [1])
Hypnosis reason for
Item
not concurrently using hypnosis for any reason
boolean
C3888013 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])