Informatie:
Fout:
ID
33440
Beschrijving
Quality of Life in Metastatic Breast Cancer (MBC) Patients in Second Line Monochemotherapy; ODM derived from: https://clinicaltrials.gov/show/NCT02403869
Link
https://clinicaltrials.gov/show/NCT02403869
Trefwoorden
Versies (1)
- 09-12-18 09-12-18 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
9 december 2018
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Breast Neoplasms NCT02403869
Eligibility Breast Neoplasms NCT02403869
- StudyEvent: Eligibility
Similar models
Eligibility Breast Neoplasms NCT02403869
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Informed Consent
Item
patients who give their written informed consent.
boolean
C0021430 (UMLS CUI [1])
Secondary malignant neoplasm of female breast | Second line Chemotherapy
Item
patients with metastatic breast cancer who start treatment with second-line monochemotherapy.
boolean
C0346993 (UMLS CUI [1])
C1710038 (UMLS CUI [2,1])
C0392920 (UMLS CUI [2,2])
C1710038 (UMLS CUI [2,1])
C0392920 (UMLS CUI [2,2])
Age | Racial group Any
Item
patients of both sexes, at least 18 years of age and of any race.
boolean
C0001779 (UMLS CUI [1])
C0034510 (UMLS CUI [2,1])
C1552551 (UMLS CUI [2,2])
C0034510 (UMLS CUI [2,1])
C1552551 (UMLS CUI [2,2])
Life Expectancy
Item
patients with life expectancy longer than or equal to 12 weeks.
boolean
C0023671 (UMLS CUI [1])
Breast adenocarcinoma HER2/Neu Negative
Item
patients with histological or cytological diagnosis of her-2/neu negative breast adenocarcinoma.
boolean
C0858252 (UMLS CUI [1,1])
C2348908 (UMLS CUI [1,2])
C2348908 (UMLS CUI [1,2])
Comprehension Questionnaires
Item
patients with ability enough to understand the questionnaires.
boolean
C0162340 (UMLS CUI [1,1])
C0034394 (UMLS CUI [1,2])
C0034394 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
pregnant or lactating women.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Study Subject Participation Status
Item
patients who are participating or have participated in a clinical trial in the last two months.
boolean
C2348568 (UMLS CUI [1])
Refusal to Participate Clinical Trial
Item
patients who refuse to participate in the study.
boolean
C1136454 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,2])