ID

26093

Description

Musculoskeletal Pain in Postmenopausal, Early Breast Cancer Patients Receiving Aromatase Inhibitor Therapy - A Pilot Study; ODM derived from: https://clinicaltrials.gov/show/NCT00653718

Link

https://clinicaltrials.gov/show/NCT00653718

Keywords

Versions (1)
  1. 10/9/17 10/9/17 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

October 9, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00653718

English

Eligibility Breast Cancer NCT00653718

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
female
Description

Gender

Data type

boolean

Alias
UMLS CUI [1]
C0079399
invasive carcinoma of the breast confirmed by needle biopsy or final pathological evaluation of the surgical specimen
Description

Invasive carcinoma of breast Needle biopsy | Invasive carcinoma of breast Surgical specimen Evaluation

Data type

boolean

Alias
UMLS CUI [1,1]
C0853879
UMLS CUI [1,2]
C0005560
UMLS CUI [2,1]
C0853879
UMLS CUI [2,2]
C1647891
UMLS CUI [2,3]
C1261322
breast cancer stage i, ii or iiia
Description

Breast Carcinoma TNM Breast tumor staging

Data type

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0474926
er and/or pr+
Description

Estrogen receptor positive | Progesterone receptor positive

Data type

boolean

Alias
UMLS CUI [1]
C0279754
UMLS CUI [2]
C0279759
no evidence of metastatic disease
Description

Neoplasm Metastasis Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0332197
post-menopausal
Description

Postmenopausal state

Data type

boolean

Alias
UMLS CUI [1]
C0232970
may or may not have received adjuvant or neoadjuvant chemotherapy
Description

Chemotherapy, Adjuvant | Chemotherapy Neoadjuvant

Data type

boolean

Alias
UMLS CUI [1]
C0085533
UMLS CUI [2,1]
C0392920
UMLS CUI [2,2]
C0600558
bilateral infiltrating carcinoma are eligible
Description

Bilateral Carcinoma Infiltrating

Data type

boolean

Alias
UMLS CUI [1,1]
C1332549
UMLS CUI [1,2]
C0332448
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
men not eligible
Description

Gender

Data type

boolean

Alias
UMLS CUI [1]
C0079399
other malignancies
Description

Malignant Neoplasms

Data type

boolean

Alias
UMLS CUI [1]
C0006826
patients who have received neoadjuvant or adjuvant endocrine therapy with tamoxifen or an aromatase inhibitor
Description

Hormone Therapy Neoadjuvant | Hormone Therapy Adjuvant | Tamoxifen | Aromatase Inhibitors

Data type

boolean

Alias
UMLS CUI [1,1]
C0279025
UMLS CUI [1,2]
C0600558
UMLS CUI [2,1]
C0279025
UMLS CUI [2,2]
C1522673
UMLS CUI [3]
C0039286
UMLS CUI [4]
C0593802
ongoing treatment with any sex hormonal therapy (these patients are eligible if this therapy is discontinued prior to entry)
Description

Sex Hormones Therapeutic procedure

Data type

boolean

Alias
UMLS CUI [1,1]
C0036884
UMLS CUI [1,2]
C0087111
therapy with hormonal agent such as raloxifene for osteoporosis
Description

Hormone Therapy Osteoporosis | Raloxifene

Data type

boolean

Alias
UMLS CUI [1,1]
C0279025
UMLS CUI [1,2]
C0029456
UMLS CUI [2]
C0244404
patients receiving glucocorticoids
Description

Glucocorticoids

Data type

boolean

Alias
UMLS CUI [1]
C0017710
psychiatric or addictive disorders
Description

Mental disorders | Addictive Behavior

Data type

boolean

Alias
UMLS CUI [1]
C0004936
UMLS CUI [2]
C0085281
inability to read english or french
Description

Lacking Able to read English Language | Lacking Able to read French language

Data type

boolean

Alias
UMLS CUI [1,1]
C0332268
UMLS CUI [1,2]
C0586740
UMLS CUI [1,3]
C0376245
UMLS CUI [2,1]
C0332268
UMLS CUI [2,2]
C0586740
UMLS CUI [2,3]
C0376246
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Similar models

Eligibility Breast Cancer NCT00653718

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Gender
Item
female
boolean
C0079399 (UMLS CUI [1])
Invasive carcinoma of breast Needle biopsy | Invasive carcinoma of breast Surgical specimen Evaluation
Item
invasive carcinoma of the breast confirmed by needle biopsy or final pathological evaluation of the surgical specimen
boolean
C0853879 (UMLS CUI [1,1])
C0005560 (UMLS CUI [1,2])
C0853879 (UMLS CUI [2,1])
C1647891 (UMLS CUI [2,2])
C1261322 (UMLS CUI [2,3])
Breast Carcinoma TNM Breast tumor staging
Item
breast cancer stage i, ii or iiia
boolean
C0678222 (UMLS CUI [1,1])
C0474926 (UMLS CUI [1,2])
Estrogen receptor positive | Progesterone receptor positive
Item
er and/or pr+
boolean
C0279754 (UMLS CUI [1])
C0279759 (UMLS CUI [2])
Neoplasm Metastasis Absent
Item
no evidence of metastatic disease
boolean
C0027627 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Postmenopausal state
Item
post-menopausal
boolean
C0232970 (UMLS CUI [1])
Chemotherapy, Adjuvant | Chemotherapy Neoadjuvant
Item
may or may not have received adjuvant or neoadjuvant chemotherapy
boolean
C0085533 (UMLS CUI [1])
C0392920 (UMLS CUI [2,1])
C0600558 (UMLS CUI [2,2])
Bilateral Carcinoma Infiltrating
Item
bilateral infiltrating carcinoma are eligible
boolean
C1332549 (UMLS CUI [1,1])
C0332448 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Gender
Item
men not eligible
boolean
C0079399 (UMLS CUI [1])
Malignant Neoplasms
Item
other malignancies
boolean
C0006826 (UMLS CUI [1])
Hormone Therapy Neoadjuvant | Hormone Therapy Adjuvant | Tamoxifen | Aromatase Inhibitors
Item
patients who have received neoadjuvant or adjuvant endocrine therapy with tamoxifen or an aromatase inhibitor
boolean
C0279025 (UMLS CUI [1,1])
C0600558 (UMLS CUI [1,2])
C0279025 (UMLS CUI [2,1])
C1522673 (UMLS CUI [2,2])
C0039286 (UMLS CUI [3])
C0593802 (UMLS CUI [4])
Sex Hormones Therapeutic procedure
Item
ongoing treatment with any sex hormonal therapy (these patients are eligible if this therapy is discontinued prior to entry)
boolean
C0036884 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
Hormone Therapy Osteoporosis | Raloxifene
Item
therapy with hormonal agent such as raloxifene for osteoporosis
boolean
C0279025 (UMLS CUI [1,1])
C0029456 (UMLS CUI [1,2])
C0244404 (UMLS CUI [2])
Glucocorticoids
Item
patients receiving glucocorticoids
boolean
C0017710 (UMLS CUI [1])
Mental disorders | Addictive Behavior
Item
psychiatric or addictive disorders
boolean
C0004936 (UMLS CUI [1])
C0085281 (UMLS CUI [2])
Lacking Able to read English Language | Lacking Able to read French language
Item
inability to read english or french
boolean
C0332268 (UMLS CUI [1,1])
C0586740 (UMLS CUI [1,2])
C0376245 (UMLS CUI [1,3])
C0332268 (UMLS CUI [2,1])
C0586740 (UMLS CUI [2,2])
C0376246 (UMLS CUI [2,3])
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