ID

31636

Description

PRostate Cancer Individual Signature Evaluation Trial in Patients Undergoing Scheduled Prostate Biopsy; ODM derived from: https://clinicaltrials.gov/show/NCT00966095

Link

https://clinicaltrials.gov/show/NCT00966095

Keywords

  1. 9/15/18 9/15/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

September 15, 2018

DOI

To request one please log in.

License

Creative Commons BY 4.0

Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Eligibility Prostate Cancer NCT00966095

Eligibility Prostate Cancer NCT00966095

Criteria
Description

Criteria

1. male over the age of 40.
Description

Gender | Age

Data type

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
2. patient is scheduled for prostate biopsy for one or more of the following reasons:
Description

Biopsy of prostate Scheduled

Data type

boolean

Alias
UMLS CUI [1,1]
C0194804
UMLS CUI [1,2]
C0205539
psa > 2.5 ng/ml
Description

Prostate specific antigen measurement

Data type

boolean

Alias
UMLS CUI [1]
C0201544
rising psa (>0.5 ng/ml/yr)
Description

Raised prostate specific antigen

Data type

boolean

Alias
UMLS CUI [1]
C0178415
lower psa value with other risk factors for prostate cancer (e.g.; family history)
Description

Prostate-Specific Antigen Value low | Risk factors Prostate carcinoma | Family history of prostate cancer

Data type

boolean

Alias
UMLS CUI [1,1]
C0138741
UMLS CUI [1,2]
C1522609
UMLS CUI [1,3]
C0205251
UMLS CUI [2,1]
C0035648
UMLS CUI [2,2]
C0600139
UMLS CUI [3]
C1532320
abnormal dre
Description

Digital Rectal Examination Abnormal

Data type

boolean

Alias
UMLS CUI [1,1]
C1384593
UMLS CUI [1,2]
C0205161
percent free psa <15%
Description

Percentage Prostate-Specific Antigen Free

Data type

boolean

Alias
UMLS CUI [1,1]
C0439165
UMLS CUI [1,2]
C0138741
UMLS CUI [1,3]
C0332296
3. no prior history of prostate cancer or prostate biopsy.
Description

Prostate carcinoma Absent | Biopsy of prostate Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C0600139
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0194804
UMLS CUI [2,2]
C0332197
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
unable or unwilling to provide informed consent
Description

Informed Consent Unable | Informed Consent Unwilling

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0558080

Similar models

Eligibility Prostate Cancer NCT00966095

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Gender | Age
Item
1. male over the age of 40.
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Biopsy of prostate Scheduled
Item
2. patient is scheduled for prostate biopsy for one or more of the following reasons:
boolean
C0194804 (UMLS CUI [1,1])
C0205539 (UMLS CUI [1,2])
Prostate specific antigen measurement
Item
psa > 2.5 ng/ml
boolean
C0201544 (UMLS CUI [1])
Raised prostate specific antigen
Item
rising psa (>0.5 ng/ml/yr)
boolean
C0178415 (UMLS CUI [1])
Prostate-Specific Antigen Value low | Risk factors Prostate carcinoma | Family history of prostate cancer
Item
lower psa value with other risk factors for prostate cancer (e.g.; family history)
boolean
C0138741 (UMLS CUI [1,1])
C1522609 (UMLS CUI [1,2])
C0205251 (UMLS CUI [1,3])
C0035648 (UMLS CUI [2,1])
C0600139 (UMLS CUI [2,2])
C1532320 (UMLS CUI [3])
Digital Rectal Examination Abnormal
Item
abnormal dre
boolean
C1384593 (UMLS CUI [1,1])
C0205161 (UMLS CUI [1,2])
Percentage Prostate-Specific Antigen Free
Item
percent free psa <15%
boolean
C0439165 (UMLS CUI [1,1])
C0138741 (UMLS CUI [1,2])
C0332296 (UMLS CUI [1,3])
Prostate carcinoma Absent | Biopsy of prostate Absent
Item
3. no prior history of prostate cancer or prostate biopsy.
boolean
C0600139 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0194804 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Informed Consent Unable | Informed Consent Unwilling
Item
unable or unwilling to provide informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial