ID

23177

Beskrivning

Responsible Party: Advanced Medical Diagnostics s.a. ClinicalTrials.gov Identifier: NCT01950871 History of Changes Other Study ID Numbers: CR2P01127 DRKS00005263 ( Registry Identifier: Deutsches Register Klinischer Studien ) Study First Received: September 19, 2013 Last Updated: January 2, 2015 Prostate Guided Biopsy Study Evaluating the Diagnostic Performance of Prostate HistoScanning; ODM derived from: https://clinicaltrials.gov/show/NCT01950871

Länk

https://clinicaltrials.gov/show/NCT01950871

Nyckelord

Versioner (1)
  1. 2017-06-26 2017-06-26 -
Uppladdad den

26 juni 2017

DOI

För en begäran logga in.

Licens

Creative Commons BY 4.0
Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Tillbaka till modellkommentarer
Itemgroup-kommentar för :

Item-kommentar för :

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

Eligibility Prostate Cancer DRKS00005263 NCT01950871 DRKS00005263

Engelsk

Eligibility Prostate Cancer NCT01950871 DRKS00005263

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
Men at risk of pca scheduled for first biopsy with serum total psa ≤ 20 ng/ml (≤ 10 ng/ml if taking 5-alpha reductase inhibitors) from maximally 3 months ago
Beskrivning

PSA

Datatyp

boolean

Alias
UMLS CUI [1]
C0138741
Signed informed consent
Beskrivning

Informed Consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
Previous prostate biopsy
Beskrivning

Previous prostate biopsy

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0194804
UMLS CUI [1,2]
C0205156
Confirmed PCa
Beskrivning

Prostate Cancer

Datatyp

boolean

Alias
UMLS CUI [1]
C0600139
PSA > 20 ng/ml (or > 10 ng/ml if taking 5-alpha reductase inhibitors)
Beskrivning

PSA: High Level

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0138741
UMLS CUI [1,2]
C0205250
active urinary tract infection
Beskrivning

Urinary tract infection

Datatyp

boolean

Alias
UMLS CUI [1]
C0042029
presence/history of any confirmed cancer
Beskrivning

Malignant Neoplasm

Datatyp

boolean

Alias
UMLS CUI [1]
C0006826
recent prostatic surgery (past 6 months)
Beskrivning

Operation on Prostate

Datatyp

boolean

Alias
UMLS CUI [1]
C0194790
history of pelvic radiotherapy
Beskrivning

Pelvic radiotherapy

Datatyp

boolean

Alias
UMLS CUI [1]
C0436276
Tillbaka till toppen

Similar models

Eligibility Prostate Cancer NCT01950871 DRKS00005263

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
PSA
Item
Men at risk of pca scheduled for first biopsy with serum total psa ≤ 20 ng/ml (≤ 10 ng/ml if taking 5-alpha reductase inhibitors) from maximally 3 months ago
boolean
C0138741 (UMLS CUI [1])
Informed Consent
Item
Signed informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Previous prostate biopsy
Item
Previous prostate biopsy
boolean
C0194804 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
Prostate Cancer
Item
Confirmed PCa
boolean
C0600139 (UMLS CUI [1])
PSA: High Level
Item
PSA > 20 ng/ml (or > 10 ng/ml if taking 5-alpha reductase inhibitors)
boolean
C0138741 (UMLS CUI [1,1])
C0205250 (UMLS CUI [1,2])
Urinary tract infection
Item
active urinary tract infection
boolean
C0042029 (UMLS CUI [1])
Malignant Neoplasm
Item
presence/history of any confirmed cancer
boolean
C0006826 (UMLS CUI [1])
Operation on Prostate
Item
recent prostatic surgery (past 6 months)
boolean
C0194790 (UMLS CUI [1])
Pelvic radiotherapy
Item
history of pelvic radiotherapy
boolean
C0436276 (UMLS CUI [1])
Tillbaka till toppen 

Kontakt

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

Hjälp

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