ID

31636

Beschreibung

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

Stichworte

  1. 15.09.18 15.09.18 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

15. September 2018

DOI

Für eine Beantragung loggen Sie sich ein.

Lizenz

Creative Commons BY 4.0

Modell Kommentare :

Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.

Itemgroup Kommentare für :

Item Kommentare für :

Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.

Eligibility Prostate Cancer NCT00966095

Eligibility Prostate Cancer NCT00966095

Criteria
Beschreibung

Criteria

1. male over the age of 40.
Beschreibung

Gender | Age

Datentyp

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:
Beschreibung

Biopsy of prostate Scheduled

Datentyp

boolean

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

Prostate specific antigen measurement

Datentyp

boolean

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

Raised prostate specific antigen

Datentyp

boolean

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

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

Datentyp

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
Beschreibung

Digital Rectal Examination Abnormal

Datentyp

boolean

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

Percentage Prostate-Specific Antigen Free

Datentyp

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.
Beschreibung

Prostate carcinoma Absent | Biopsy of prostate Absent

Datentyp

boolean

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

Exclusion Criteria

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

Informed Consent Unable | Informed Consent Unwilling

Datentyp

boolean

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

Ähnliche Modelle

Eligibility Prostate Cancer NCT00966095

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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])

Benutzen Sie dieses Formular für Rückmeldungen, Fragen und Verbesserungsvorschläge.

Mit * gekennzeichnete Felder sind notwendig.

Benötigen Sie Hilfe bei der Suche? Um mehr Details zu erfahren und die Suche effektiver nutzen zu können schauen Sie sich doch das entsprechende Video auf unserer Tutorial Seite an.

Zum Video