Informações:
Falhas:
ID
42225
Descrição
Adjuvant Treatment of Breast Cancer With 1-3 Aflicted Lymph Nodes; ODM derived from: https://clinicaltrials.gov/show/NCT00668616
Link
https://clinicaltrials.gov/show/NCT00668616
Palavras-chave
Versões (2)
- 01/02/2016 01/02/2016 -
- 13/04/2021 13/04/2021 - Dr. rer. medic Philipp Neuhaus
Transferido a
13 de abril de 2021
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00668616
Eligibility Breast Cancer NCT00668616
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00668616
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Breast Cancer staging
Item
women with histologically proven breast cancer (pt1/pt2/pt3, pn1, n0)
boolean
C0474926 (UMLS CUI [1])
ecog performance status
Item
ecog performance status 0-1
boolean
C1520224 (UMLS CUI [1])
Adjuvant therapy
Item
start of adjuvant therapy not later than 4 weeks after surgery
boolean
C0677850 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
Hematological status
Item
hematology: platelets at least 100xgpt/l, neutrophiles at least 2xgpt/l
boolean
C0032181 (UMLS CUI [1])
C2238207 (UMLS CUI [2])
C2238207 (UMLS CUI [2])
Liver function
Item
normal liver function as defined by: bilirubine till 1.5 x normal value, sgot/sgpt till 1.25 x normal value
boolean
C1278039 (UMLS CUI [1])
C0201836 (UMLS CUI [2])
C0201899 (UMLS CUI [3])
C0201836 (UMLS CUI [2])
C0201899 (UMLS CUI [3])
Kidney function
Item
normal kidney function as defined by: creatine till 1.5 x normal value
boolean
C0201976 (UMLS CUI [1])
Gynaecological status
Item
negative pregnancy test for patients before menopause and effective contraception
boolean
C0032976 (UMLS CUI [1])
C0700589 (UMLS CUI [2])
C0700589 (UMLS CUI [2])
informed consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Therapy
Item
prior radiation, chemotherapy, hormontherapy and immunotherapy
boolean
C0851346 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
C0279025 (UMLS CUI [3,1])
C0021083 (UMLS CUI [3,2])
C0392920 (UMLS CUI [2])
C0279025 (UMLS CUI [3,1])
C0021083 (UMLS CUI [3,2])
Staging: Lymph nodes
Item
patients with more than 3 afflicted lymph nodes
boolean
C2216721 (UMLS CUI [1])
Staging: lymph nodes
Item
afflicted lymph nodes on the cantralateal side and/or afflicted supraclavicular or intraclavicular lymph nodes
boolean
C0024204 (UMLS CUI [1,1])
C0441988 (UMLS CUI [1,2])
C0229730 (UMLS CUI [2])
C0229743 (UMLS CUI [3])
C0441988 (UMLS CUI [1,2])
C0229730 (UMLS CUI [2])
C0229743 (UMLS CUI [3])
Further breast malignancies
Item
bilateral breast cancer or second carcinoma of the breast
boolean
C0281267 (UMLS CUI [1])
C0346993 (UMLS CUI [2])
C0346993 (UMLS CUI [2])
inflammatory breast cancer, distant metastases
Item
inflammatory breast cancer and/or distant metastases
boolean
C0278601 (UMLS CUI [1])
C1268959 (UMLS CUI [2])
C1268959 (UMLS CUI [2])
peripheral neuropathy
Item
existing clinically relevant peripheral neuropathie
boolean
C0031117 (UMLS CUI [1])
Cardiac status
Item
heart infection during the last 6 months or therapeutically not compensated heart failure or cardiac arrhythmias of at least lown ii
boolean
C1096253 (UMLS CUI [1])
C0018801 (UMLS CUI [2])
C0003811 (UMLS CUI [3])
C0018801 (UMLS CUI [2])
C0003811 (UMLS CUI [3])
Comorbidity
Item
patients with active infections and/or not controlled hypercalcemia
boolean
C3714514 (UMLS CUI [1])
C0020437 (UMLS CUI [2])
C0020437 (UMLS CUI [2])
gynaecological status
Item
pregnant or breastfeeding women or women of child-bearing age who do not use effictive contrazeptiva
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0700589 (UMLS CUI [3])
C0006147 (UMLS CUI [2])
C0700589 (UMLS CUI [3])