Eligibility Prostate Cancer NCT01687049

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically diagnosis of prostate adenocarcinoma
Description

Adenocarcinoma of prostate

Data type

boolean

Alias
UMLS CUI [1]
C0007112
being monitored by active surveillance for favourable risk prostate cancer
Description

Surveillance Risk Prostate carcinoma

Data type

boolean

Alias
UMLS CUI [1,1]
C0733511
UMLS CUI [1,2]
C0035647
UMLS CUI [1,3]
C0600139
tumour material from most recent prostate biopsy available with sample
Description

Biopsy of prostate Tumor tissue sample Available

Data type

boolean

Alias
UMLS CUI [1,1]
C0194804
UMLS CUI [1,2]
C0475358
UMLS CUI [1,3]
C0470187
scheduled to have an active surveillance mandated transrectal ultrasound (trus) guided biopsy within 6 - 12 months of day 1 of the study
Description

Transrectal ultrasound Biopsy Scheduled

Data type

boolean

Alias
UMLS CUI [1,1]
C0373345
UMLS CUI [1,2]
C0005558
UMLS CUI [1,3]
C0205539
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
previous malignancy in the past 5 years
Description

Malignant Neoplasms Previous

Data type

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0205156
no previous or concurrent treatment for prostate cancer
Description

Therapeutic procedure Prostate carcinoma

Data type

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0600139
inability to undergo trus biopsy
Description

Transrectal ultrasound Biopsy Receive Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C0373345
UMLS CUI [1,2]
C0005558
UMLS CUI [1,3]
C1514756
UMLS CUI [1,4]
C1299582
ecog > 2
Description

ECOG performance status

Data type

boolean

Alias
UMLS CUI [1]
C1520224
known or previous history of liver disease
Description

Liver disease

Data type

boolean

Alias
UMLS CUI [1]
C0023895

Similar models

Eligibility Prostate Cancer NCT01687049

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Adenocarcinoma of prostate
Item
histologically diagnosis of prostate adenocarcinoma
boolean
C0007112 (UMLS CUI [1])
Surveillance Risk Prostate carcinoma
Item
being monitored by active surveillance for favourable risk prostate cancer
boolean
C0733511 (UMLS CUI [1,1])
C0035647 (UMLS CUI [1,2])
C0600139 (UMLS CUI [1,3])
Biopsy of prostate Tumor tissue sample Available
Item
tumour material from most recent prostate biopsy available with sample
boolean
C0194804 (UMLS CUI [1,1])
C0475358 (UMLS CUI [1,2])
C0470187 (UMLS CUI [1,3])
Transrectal ultrasound Biopsy Scheduled
Item
scheduled to have an active surveillance mandated transrectal ultrasound (trus) guided biopsy within 6 - 12 months of day 1 of the study
boolean
C0373345 (UMLS CUI [1,1])
C0005558 (UMLS CUI [1,2])
C0205539 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Malignant Neoplasms Previous
Item
previous malignancy in the past 5 years
boolean
C0006826 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
Therapeutic procedure Prostate carcinoma
Item
no previous or concurrent treatment for prostate cancer
boolean
C0087111 (UMLS CUI [1,1])
C0600139 (UMLS CUI [1,2])
Transrectal ultrasound Biopsy Receive Unable
Item
inability to undergo trus biopsy
boolean
C0373345 (UMLS CUI [1,1])
C0005558 (UMLS CUI [1,2])
C1514756 (UMLS CUI [1,3])
C1299582 (UMLS CUI [1,4])
ECOG performance status
Item
ecog > 2
boolean
C1520224 (UMLS CUI [1])
Liver disease
Item
known or previous history of liver disease
boolean
C0023895 (UMLS CUI [1])