Informatie:
Fout:
ID
16206
Beschrijving
Pemetrexed as First Line Chemotherapy for Advanced Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00065533
Link
https://clinicaltrials.gov/show/NCT00065533
Trefwoorden
Versies (1)
- 05-07-16 05-07-16 -
Geüploaded op
5 juli 2016
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00065533
Eligibility Breast Cancer NCT00065533
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00065533
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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])
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])
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])
C0545082 (UMLS CUI [1,2])
C0031834 (UMLS CUI [1,3])
Pregnancy | Breast Feeding
Item
to be pregnant or breastfeeding.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
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])
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])
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])
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])
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])