ID

16247

Description

Complementary Therapies for the Reduction of Side Effects During Chemotherapy for Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00160901

Link

https://clinicaltrials.gov/show/NCT00160901

Keywords

Versions (1)
  1. 7/7/16 7/7/16 -
Uploaded on

July 7, 2016

DOI

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License

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00160901

English

Eligibility Breast Cancer NCT00160901

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
indication for chemotherapy for breast cancer for at least 3 cycles
Description

Indication Chemotherapy cycle Breast Carcinoma

Data type

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C1302181
UMLS CUI [1,3]
C0678222
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
prior chemotherapy within 12 months
Description

Prior Chemotherapy

Data type

boolean

Alias
UMLS CUI [1]
C1514457
use of herbal or nutritional supplements or other complementary or alternative medications ≥ 7 days prior to start of chemotherapy and during the trial
Description

Herbal Drugs Supplement | Dietary Supplements | Pharmaceutical Preparations Supplemental | Pharmaceutical Preparations Alternative | Chemotherapy

Data type

boolean

Alias
UMLS CUI [1,1]
C1360419
UMLS CUI [1,2]
C2348609
UMLS CUI [2]
C0242295
UMLS CUI [3,1]
C0013227
UMLS CUI [3,2]
C2348609
UMLS CUI [4,1]
C0013227
UMLS CUI [4,2]
C1523987
UMLS CUI [5]
C0392920
allergy to study medication
Description

Hypersensitivity Investigational New Drug

Data type

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0013230
selenium intoxication
Description

Selenium Intoxication

Data type

boolean

Alias
UMLS CUI [1,1]
C0036581
UMLS CUI [1,2]
C0728899
current use of cumarins or other medication influencing the coagulation system
Description

coumarin | Pharmaceutical Preparations Affecting Blood coagulation System

Data type

boolean

Alias
UMLS CUI [1]
C0010206
UMLS CUI [2,1]
C0013227
UMLS CUI [2,2]
C0392760
UMLS CUI [2,3]
C0005778
UMLS CUI [2,4]
C0449913
edema in case of impaired cardial or renal function
Description

Edema | Decreased cardiac function | Renal Insufficiency

Data type

boolean

Alias
UMLS CUI [1]
C0013604
UMLS CUI [2]
C0232166
UMLS CUI [3]
C1565489
other severe medical condition
Description

Other medical condition Severe

Data type

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0205082
psychiatric or central neurological disorders
Description

Mental disorders | CNS disorder

Data type

boolean

Alias
UMLS CUI [1]
C0004936
UMLS CUI [2]
C0007682
regular fluid intake < 2000 ml per day
Description

Fluid intake Regular per day

Data type

boolean

Alias
UMLS CUI [1,1]
C0429791
UMLS CUI [1,2]
C0205272
UMLS CUI [1,3]
C0439505
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Similar models

Eligibility Breast Cancer NCT00160901

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Indication Chemotherapy cycle Breast Carcinoma
Item
indication for chemotherapy for breast cancer for at least 3 cycles
boolean
C3146298 (UMLS CUI [1,1])
C1302181 (UMLS CUI [1,2])
C0678222 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Prior Chemotherapy
Item
prior chemotherapy within 12 months
boolean
C1514457 (UMLS CUI [1])
Herbal Drugs Supplement | Dietary Supplements | Pharmaceutical Preparations Supplemental | Pharmaceutical Preparations Alternative | Chemotherapy
Item
use of herbal or nutritional supplements or other complementary or alternative medications ≥ 7 days prior to start of chemotherapy and during the trial
boolean
C1360419 (UMLS CUI [1,1])
C2348609 (UMLS CUI [1,2])
C0242295 (UMLS CUI [2])
C0013227 (UMLS CUI [3,1])
C2348609 (UMLS CUI [3,2])
C0013227 (UMLS CUI [4,1])
C1523987 (UMLS CUI [4,2])
C0392920 (UMLS CUI [5])
Hypersensitivity Investigational New Drug
Item
allergy to study medication
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
Selenium Intoxication
Item
selenium intoxication
boolean
C0036581 (UMLS CUI [1,1])
C0728899 (UMLS CUI [1,2])
coumarin | Pharmaceutical Preparations Affecting Blood coagulation System
Item
current use of cumarins or other medication influencing the coagulation system
boolean
C0010206 (UMLS CUI [1])
C0013227 (UMLS CUI [2,1])
C0392760 (UMLS CUI [2,2])
C0005778 (UMLS CUI [2,3])
C0449913 (UMLS CUI [2,4])
Edema | Decreased cardiac function | Renal Insufficiency
Item
edema in case of impaired cardial or renal function
boolean
C0013604 (UMLS CUI [1])
C0232166 (UMLS CUI [2])
C1565489 (UMLS CUI [3])
Other medical condition Severe
Item
other severe medical condition
boolean
C3843040 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Mental disorders | CNS disorder
Item
psychiatric or central neurological disorders
boolean
C0004936 (UMLS CUI [1])
C0007682 (UMLS CUI [2])
Fluid intake Regular per day
Item
regular fluid intake < 2000 ml per day
boolean
C0429791 (UMLS CUI [1,1])
C0205272 (UMLS CUI [1,2])
C0439505 (UMLS CUI [1,3])
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