ID

26093

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT00653718

Nyckelord

  1. 2017-10-09 2017-10-09 -
Rättsinnehavare

See clinicaltrials.gov

Uppladdad den

9 oktober 2017

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00653718

Eligibility Breast Cancer NCT00653718

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
female
Beskrivning

Gender

Datatyp

boolean

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

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

Datatyp

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
Beskrivning

Breast Carcinoma TNM Breast tumor staging

Datatyp

boolean

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

Estrogen receptor positive | Progesterone receptor positive

Datatyp

boolean

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

Neoplasm Metastasis Absent

Datatyp

boolean

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

Postmenopausal state

Datatyp

boolean

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

Chemotherapy, Adjuvant | Chemotherapy Neoadjuvant

Datatyp

boolean

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

Bilateral Carcinoma Infiltrating

Datatyp

boolean

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

Exclusion Criteria

Alias
UMLS CUI
C0680251
men not eligible
Beskrivning

Gender

Datatyp

boolean

Alias
UMLS CUI [1]
C0079399
other malignancies
Beskrivning

Malignant Neoplasms

Datatyp

boolean

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

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

Datatyp

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)
Beskrivning

Sex Hormones Therapeutic procedure

Datatyp

boolean

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

Hormone Therapy Osteoporosis | Raloxifene

Datatyp

boolean

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

Glucocorticoids

Datatyp

boolean

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

Mental disorders | Addictive Behavior

Datatyp

boolean

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

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

Datatyp

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

Similar models

Eligibility Breast Cancer NCT00653718

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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