ID

30059

Description

Green Tea in Breast Cancer Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00949923

Link

https://clinicaltrials.gov/show/NCT00949923

Keywords

  1. 5/7/18 5/7/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

May 7, 2018

DOI

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License

Creative Commons BY 4.0

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Eligibility Incident Breast Cancer NCT00949923

Eligibility Incident Breast Cancer NCT00949923

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
postmenopausal (at least 2 years since last menstrual period) or age 55 or older if prior hysterectomy
Description

Postmenopausal state | Age | Hysterectomy

Data type

boolean

Alias
UMLS CUI [1]
C0232970
UMLS CUI [2]
C0001779
UMLS CUI [3]
C0020699
non-current (not with past 6 months) user of menopausal hormones
Description

Hormone replacement therapy Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C0282402
UMLS CUI [1,2]
C0332197
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.
Description

Mammography abnormal Consistent with Breast Carcinoma | Patient need for Biopsy BIRAD | Liver Function Tests | Screening questionnaire

Data type

boolean

Alias
UMLS CUI [1,1]
C0262365
UMLS CUI [1,2]
C0332290
UMLS CUI [1,3]
C0678222
UMLS CUI [2,1]
C0686904
UMLS CUI [2,2]
C0005558
UMLS CUI [2,3]
C1511314
UMLS CUI [3]
C0023901
UMLS CUI [4]
C1134635
diagnosed with incident breast cancer on the diagnostic biopsy is required for inclusion in the egcg or control treatment groups.
Description

Breast Carcinoma Biopsy

Data type

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0005558
non-green tea drinker (less than monthly) - this criteria does not apply to black tea or herbal tea
Description

Green tea Drinking Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C1384640
UMLS CUI [1,2]
C0684271
UMLS CUI [1,3]
C0332197
provided written informed consent
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
green tea drinker (once per month or more)
Description

Green tea Drinking

Data type

boolean

Alias
UMLS CUI [1,1]
C1384640
UMLS CUI [1,2]
C0684271
history of breast cancer or other cancer including a prior diagnosis of any type of incident breast cancer.
Description

Medical History Breast Carcinoma | H/O: malignant neoplasm

Data type

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0678222
UMLS CUI [2]
C0455471
known allergy to tea
Description

Hypersensitivity Tea

Data type

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0039400
abnormal liver enzymes (plus or minus 10% of the normal ranges).
Description

Liver enzymes abnormal | Elevated liver enzymes | Liver enzymes Decreased

Data type

boolean

Alias
UMLS CUI [1]
C0438237
UMLS CUI [2]
C0235996
UMLS CUI [3,1]
C1287351
UMLS CUI [3,2]
C0205216

Similar models

Eligibility Incident Breast Cancer NCT00949923

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
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])
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])
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])
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])
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])
Informed Consent
Item
provided written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Green tea Drinking
Item
green tea drinker (once per month or more)
boolean
C1384640 (UMLS CUI [1,1])
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])
Hypersensitivity Tea
Item
known allergy to tea
boolean
C0020517 (UMLS CUI [1,1])
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])

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