Informações:
Falhas:
ID
26093
Descrição
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
Palavras-chave
Versões (1)
- 09/10/2017 09/10/2017 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
9 de outubro de 2017
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00653718
Eligibility Breast Cancer NCT00653718
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00653718
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
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])
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])
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])
C0279759 (UMLS CUI [2])
Neoplasm Metastasis Absent
Item
no evidence of metastatic disease
boolean
C0027627 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
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])
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])
C0332448 (UMLS CUI [1,2])
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])
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])
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])
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])
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])
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])