Informatie:
Fout:
ID
30059
Beschrijving
Green Tea in Breast Cancer Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00949923
Link
https://clinicaltrials.gov/show/NCT00949923
Trefwoorden
Versies (1)
- 07-05-18 07-05-18 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
7 mei 2018
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Incident Breast Cancer NCT00949923
Eligibility Incident Breast Cancer NCT00949923
- StudyEvent: Eligibility
Similar models
Eligibility Incident Breast Cancer NCT00949923
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Postmenopausal state | Age | Hysterectomy
Item
postmenopausal (at least 2 years since last menstrual period) or age 55 or older if prior hysterectomy
boolean
C0232970 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0020699 (UMLS CUI [3])
C0001779 (UMLS CUI [2])
C0020699 (UMLS CUI [3])
Hormone replacement therapy Absent
Item
non-current (not with past 6 months) user of menopausal hormones
boolean
C0282402 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,2])
Mammography abnormal Consistent with Breast Carcinoma | Patient need for Biopsy BIRAD | Liver Function Tests | Screening questionnaire
Item
mammographic abnormality consistent with any type of incident breast cancer necessitating a diagnostic biopsy (birad iv(b), (c) or v) will be sufficient to draw baseline lft and complete screening questionnaire. unless the biopsy confirms incident breast cancer, such subjects will not be included in further research interventions and they will not serve as egcg treated or control subjects.
boolean
C0262365 (UMLS CUI [1,1])
C0332290 (UMLS CUI [1,2])
C0678222 (UMLS CUI [1,3])
C0686904 (UMLS CUI [2,1])
C0005558 (UMLS CUI [2,2])
C1511314 (UMLS CUI [2,3])
C0023901 (UMLS CUI [3])
C1134635 (UMLS CUI [4])
C0332290 (UMLS CUI [1,2])
C0678222 (UMLS CUI [1,3])
C0686904 (UMLS CUI [2,1])
C0005558 (UMLS CUI [2,2])
C1511314 (UMLS CUI [2,3])
C0023901 (UMLS CUI [3])
C1134635 (UMLS CUI [4])
Breast Carcinoma Biopsy
Item
diagnosed with incident breast cancer on the diagnostic biopsy is required for inclusion in the egcg or control treatment groups.
boolean
C0678222 (UMLS CUI [1,1])
C0005558 (UMLS CUI [1,2])
C0005558 (UMLS CUI [1,2])
Green tea Drinking Absent
Item
non-green tea drinker (less than monthly) - this criteria does not apply to black tea or herbal tea
boolean
C1384640 (UMLS CUI [1,1])
C0684271 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C0684271 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Informed Consent
Item
provided written informed consent
boolean
C0021430 (UMLS CUI [1])
Green tea Drinking
Item
green tea drinker (once per month or more)
boolean
C1384640 (UMLS CUI [1,1])
C0684271 (UMLS CUI [1,2])
C0684271 (UMLS CUI [1,2])
Medical History Breast Carcinoma | H/O: malignant neoplasm
Item
history of breast cancer or other cancer including a prior diagnosis of any type of incident breast cancer.
boolean
C0262926 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
C0455471 (UMLS CUI [2])
C0678222 (UMLS CUI [1,2])
C0455471 (UMLS CUI [2])
Hypersensitivity Tea
Item
known allergy to tea
boolean
C0020517 (UMLS CUI [1,1])
C0039400 (UMLS CUI [1,2])
C0039400 (UMLS CUI [1,2])
Liver enzymes abnormal | Elevated liver enzymes | Liver enzymes Decreased
Item
abnormal liver enzymes (plus or minus 10% of the normal ranges).
boolean
C0438237 (UMLS CUI [1])
C0235996 (UMLS CUI [2])
C1287351 (UMLS CUI [3,1])
C0205216 (UMLS CUI [3,2])
C0235996 (UMLS CUI [2])
C1287351 (UMLS CUI [3,1])
C0205216 (UMLS CUI [3,2])