Informações:
Falhas:
ID
43638
Descrição
Fatigue Caused by Chemotherapy in Women Who Have Undergone Surgery for Breast Cancer and in Healthy Volunteers; ODM derived from: https://clinicaltrials.gov/show/NCT00909662
Link
https://clinicaltrials.gov/show/NCT00909662
Palavras-chave
Versões (2)
- 26/10/2017 26/10/2017 -
- 20/09/2021 20/09/2021 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
20 de setembro de 2021
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00909662
Eligibility Breast Cancer NCT00909662
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00909662
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Criteria Fulfill
Item
meets either of the following criteria:
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
C1550543 (UMLS CUI [1,2])
Operative Surgical Procedures Completed | Breast Carcinoma TNM Breast tumor staging
Item
has completed surgery for stage i-iii breast cancer and meets the following criteria:
boolean
C0543467 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C0678222 (UMLS CUI [2,1])
C0474926 (UMLS CUI [2,2])
C0205197 (UMLS CUI [1,2])
C0678222 (UMLS CUI [2,1])
C0474926 (UMLS CUI [2,2])
Exclusion | Excision of axillary lymph nodes Bilateral
Item
no bilateral axillary dissection
boolean
C2828389 (UMLS CUI [1])
C0193867 (UMLS CUI [2,1])
C0238767 (UMLS CUI [2,2])
C0193867 (UMLS CUI [2,1])
C0238767 (UMLS CUI [2,2])
Disease Free of
Item
clinically free of active disease
boolean
C0012634 (UMLS CUI [1,1])
C0332296 (UMLS CUI [1,2])
C0332296 (UMLS CUI [1,2])
Adjuvant Chemotherapy Planned | Breast Carcinoma Operable
Item
planning to receive adjuvant chemotherapy for operable breast cancer
boolean
C0085533 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0678222 (UMLS CUI [2,1])
C0205188 (UMLS CUI [2,2])
C1301732 (UMLS CUI [1,2])
C0678222 (UMLS CUI [2,1])
C0205188 (UMLS CUI [2,2])
Friend Age matched | Relative Age matched
Item
friend or relative of patient matched for age (± 10 years) (control)
boolean
C0079382 (UMLS CUI [1,1])
C0001779 (UMLS CUI [1,2])
C0150103 (UMLS CUI [1,3])
C0080103 (UMLS CUI [2,1])
C0001779 (UMLS CUI [2,2])
C0150103 (UMLS CUI [2,3])
C0001779 (UMLS CUI [1,2])
C0150103 (UMLS CUI [1,3])
C0080103 (UMLS CUI [2,1])
C0001779 (UMLS CUI [2,2])
C0150103 (UMLS CUI [2,3])
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])
C0449438 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,3])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Menopausal Status Known
Item
known menopausal status
boolean
C3829127 (UMLS CUI [1,1])
C0205309 (UMLS CUI [1,2])
C0205309 (UMLS CUI [1,2])
Able to read English Language
Item
able to read english
boolean
C0586740 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
C0376245 (UMLS CUI [1,2])
Exclusion Criteria | Cardiovascular Diseases | Cerebrovascular accident | Polyneuropathy | Muscular Atrophy | Myasthenic Syndrome | Pulmonary function impairment
Item
no history of significant cardiovascular disease or stroke, polyneuropathy, amyotrophy, myosthenic syndrome, or pulmonary compromise
boolean
C0680251 (UMLS CUI [1])
C0007222 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
C0152025 (UMLS CUI [4])
C0026846 (UMLS CUI [5])
C0549225 (UMLS CUI [6])
C0858943 (UMLS CUI [7])
C0007222 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
C0152025 (UMLS CUI [4])
C0026846 (UMLS CUI [5])
C0549225 (UMLS CUI [6])
C0858943 (UMLS CUI [7])
Depressive disorder
Item
prior depression allowed provided that it was not significant
boolean
C0011581 (UMLS CUI [1])
Assessment Quantity Willing
Item
willing to come to the cleveland clinic for 3 assessments
boolean
C1516048 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0600109 (UMLS CUI [1,3])
C1265611 (UMLS CUI [1,2])
C0600109 (UMLS CUI [1,3])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
ID.15
Item
see disease characteristics
boolean