ID

34260

Beschrijving

Efficacy and Safety Study of ELIGARD 22.5mg With Prostate Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01511874

Link

https://clinicaltrials.gov/show/NCT01511874

Trefwoorden

  1. 16-01-19 16-01-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

16 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Prostate Cancer NCT01511874

Eligibility Prostate Cancer NCT01511874

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
male of 20 years or above
Beschrijving

Gender | Age

Datatype

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
subject with prostate cancer with tnm stage t2~4nxmx
Beschrijving

Prostate carcinoma TNM Prostate tumor staging

Datatype

boolean

Alias
UMLS CUI [1,1]
C0600139
UMLS CUI [1,2]
C0474935
blood testosterone concentration ≥ 100ng/dl
Beschrijving

Blood testosterone measurement

Datatype

boolean

Alias
UMLS CUI [1]
C0853134
bilirubin ≤ 1.5xuln, transaminase ≤ 2.5xuln
Beschrijving

Serum total bilirubin measurement | Transaminases Measurement

Datatype

boolean

Alias
UMLS CUI [1]
C1278039
UMLS CUI [2,1]
C0002594
UMLS CUI [2,2]
C0242485
who ecog performance status ≤ 2
Beschrijving

WHO performance status scale | ECOG performance status

Datatype

boolean

Alias
UMLS CUI [1]
C1298650
UMLS CUI [2]
C1520224
signed written informed consent
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
hormone-refractory prostate cancer
Beschrijving

Hormone refractory prostate cancer

Datatype

boolean

Alias
UMLS CUI [1]
C1328504
brain metastasis
Beschrijving

Metastatic malignant neoplasm to brain

Datatype

boolean

Alias
UMLS CUI [1]
C0220650
another primary malignant tumor except for prostate cancer
Beschrijving

Primary tumor Other | Exception Prostate carcinoma

Datatype

boolean

Alias
UMLS CUI [1,1]
C0677930
UMLS CUI [1,2]
C0205394
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0600139
other conditions which in the opinion of the investigator preclude enrollment into the study
Beschrijving

Condition Study Subject Participation Status Excluded

Datatype

boolean

Alias
UMLS CUI [1,1]
C0348080
UMLS CUI [1,2]
C2348568
UMLS CUI [1,3]
C0332196

Similar models

Eligibility Prostate Cancer NCT01511874

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Gender | Age
Item
male of 20 years or above
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Prostate carcinoma TNM Prostate tumor staging
Item
subject with prostate cancer with tnm stage t2~4nxmx
boolean
C0600139 (UMLS CUI [1,1])
C0474935 (UMLS CUI [1,2])
Blood testosterone measurement
Item
blood testosterone concentration ≥ 100ng/dl
boolean
C0853134 (UMLS CUI [1])
Serum total bilirubin measurement | Transaminases Measurement
Item
bilirubin ≤ 1.5xuln, transaminase ≤ 2.5xuln
boolean
C1278039 (UMLS CUI [1])
C0002594 (UMLS CUI [2,1])
C0242485 (UMLS CUI [2,2])
WHO performance status scale | ECOG performance status
Item
who ecog performance status ≤ 2
boolean
C1298650 (UMLS CUI [1])
C1520224 (UMLS CUI [2])
Informed Consent
Item
signed written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Hormone refractory prostate cancer
Item
hormone-refractory prostate cancer
boolean
C1328504 (UMLS CUI [1])
Metastatic malignant neoplasm to brain
Item
brain metastasis
boolean
C0220650 (UMLS CUI [1])
Primary tumor Other | Exception Prostate carcinoma
Item
another primary malignant tumor except for prostate cancer
boolean
C0677930 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0600139 (UMLS CUI [2,2])
Condition Study Subject Participation Status Excluded
Item
other conditions which in the opinion of the investigator preclude enrollment into the study
boolean
C0348080 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C0332196 (UMLS CUI [1,3])

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