ID

16206

Description

Pemetrexed as First Line Chemotherapy for Advanced Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00065533

Link

https://clinicaltrials.gov/show/NCT00065533

Keywords

  1. 7/5/16 7/5/16 -
Uploaded on

July 5, 2016

DOI

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License

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00065533

Eligibility Breast Cancer NCT00065533

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
be at least 18 years of old.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
have been diagnosed with breast cancer
Description

Breast Carcinoma

Data type

boolean

Alias
UMLS CUI [1]
C0678222
at least one year disease-free interval after initial treatment.
Description

Status post Therapeutic procedure Initial | Interval Disease Free

Data type

boolean

Alias
UMLS CUI [1,1]
C0231290
UMLS CUI [1,2]
C0087111
UMLS CUI [1,3]
C0205265
UMLS CUI [2,1]
C1272706
UMLS CUI [2,2]
C0012634
UMLS CUI [2,3]
C0332296
have pre-study laboratory tests that are within the requirements of this study.
Description

Laboratory test finding Study Protocol suitable

Data type

boolean

Alias
UMLS CUI [1,1]
C0587081
UMLS CUI [1,2]
C2348563
UMLS CUI [1,3]
C3900053
be able to visit the doctor's office weekly during the treatment period.
Description

Ability Visit Doctor's Office

Data type

boolean

Alias
UMLS CUI [1,1]
C0085732
UMLS CUI [1,2]
C0545082
UMLS CUI [1,3]
C0031834
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
to be pregnant or breastfeeding.
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
to be currently taking aspirin or aspirin- like medicine and unable to stop for a few days during each cycle of therapy.
Description

taking aspirin | Intake Aspirin-Like Agents | medication stopping Unable

Data type

boolean

Alias
UMLS CUI [1]
C2054131
UMLS CUI [2,1]
C1512806
UMLS CUI [2,2]
C0085847
UMLS CUI [3,1]
C0850893
UMLS CUI [3,2]
C1299582
to have received prior chemotherapy for the treatment of metastatic cancer. patients may have received prior hormonal treatment.
Description

Prior Chemotherapy Metastatic Neoplasm | Prior Hormone Therapy

Data type

boolean

Alias
UMLS CUI [1,1]
C1514457
UMLS CUI [1,2]
C2939420
UMLS CUI [2]
C1514460
to have another illness that your doctor thinks would make you unable to participate.
Description

Comorbidity Study Subject Participation Status Limited

Data type

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C2348568
UMLS CUI [1,3]
C0439801
to be unable or not willing to take folic acid and vitamin b12.
Description

Unable to take Folic Acid | Unable to take Vitamin B 12 | Intake Folic Acid Unwilling | Intake Vitamin B 12 Unwilling

Data type

boolean

Alias
UMLS CUI [1,1]
C4074979
UMLS CUI [1,2]
C0016410
UMLS CUI [2,1]
C4074979
UMLS CUI [2,2]
C0042845
UMLS CUI [3,1]
C1512806
UMLS CUI [3,2]
C0016410
UMLS CUI [3,3]
C0558080
UMLS CUI [4,1]
C1512806
UMLS CUI [4,2]
C0042845
UMLS CUI [4,3]
C0558080

Similar models

Eligibility Breast Cancer NCT00065533

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
be at least 18 years of old.
boolean
C0001779 (UMLS CUI [1])
Breast Carcinoma
Item
have been diagnosed with breast cancer
boolean
C0678222 (UMLS CUI [1])
Status post Therapeutic procedure Initial | Interval Disease Free
Item
at least one year disease-free interval after initial treatment.
boolean
C0231290 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C0205265 (UMLS CUI [1,3])
C1272706 (UMLS CUI [2,1])
C0012634 (UMLS CUI [2,2])
C0332296 (UMLS CUI [2,3])
Laboratory test finding Study Protocol suitable
Item
have pre-study laboratory tests that are within the requirements of this study.
boolean
C0587081 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C3900053 (UMLS CUI [1,3])
Ability Visit Doctor's Office
Item
be able to visit the doctor's office weekly during the treatment period.
boolean
C0085732 (UMLS CUI [1,1])
C0545082 (UMLS CUI [1,2])
C0031834 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Pregnancy | Breast Feeding
Item
to be pregnant or breastfeeding.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
taking aspirin | Intake Aspirin-Like Agents | medication stopping Unable
Item
to be currently taking aspirin or aspirin- like medicine and unable to stop for a few days during each cycle of therapy.
boolean
C2054131 (UMLS CUI [1])
C1512806 (UMLS CUI [2,1])
C0085847 (UMLS CUI [2,2])
C0850893 (UMLS CUI [3,1])
C1299582 (UMLS CUI [3,2])
Prior Chemotherapy Metastatic Neoplasm | Prior Hormone Therapy
Item
to have received prior chemotherapy for the treatment of metastatic cancer. patients may have received prior hormonal treatment.
boolean
C1514457 (UMLS CUI [1,1])
C2939420 (UMLS CUI [1,2])
C1514460 (UMLS CUI [2])
Comorbidity Study Subject Participation Status Limited
Item
to have another illness that your doctor thinks would make you unable to participate.
boolean
C0009488 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
Unable to take Folic Acid | Unable to take Vitamin B 12 | Intake Folic Acid Unwilling | Intake Vitamin B 12 Unwilling
Item
to be unable or not willing to take folic acid and vitamin b12.
boolean
C4074979 (UMLS CUI [1,1])
C0016410 (UMLS CUI [1,2])
C4074979 (UMLS CUI [2,1])
C0042845 (UMLS CUI [2,2])
C1512806 (UMLS CUI [3,1])
C0016410 (UMLS CUI [3,2])
C0558080 (UMLS CUI [3,3])
C1512806 (UMLS CUI [4,1])
C0042845 (UMLS CUI [4,2])
C0558080 (UMLS CUI [4,3])

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