ID

31636

Descripción

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

Palabras clave

  1. 15/9/18 15/9/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

15 de septiembre de 2018

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Prostate Cancer NCT00966095

Eligibility Prostate Cancer NCT00966095

Criteria
Descripción

Criteria

1. male over the age of 40.
Descripción

Gender | Age

Tipo de datos

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:
Descripción

Biopsy of prostate Scheduled

Tipo de datos

boolean

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

Prostate specific antigen measurement

Tipo de datos

boolean

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

Raised prostate specific antigen

Tipo de datos

boolean

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

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

Tipo de datos

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
Descripción

Digital Rectal Examination Abnormal

Tipo de datos

boolean

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

Percentage Prostate-Specific Antigen Free

Tipo de datos

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.
Descripción

Prostate carcinoma Absent | Biopsy of prostate Absent

Tipo de datos

boolean

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

Exclusion Criteria

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

Informed Consent Unable | Informed Consent Unwilling

Tipo de datos

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
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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])

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