ID

34469

Beschrijving

Study of Current Practice Which Compare the Rate of Prostate Cancer by Using 2 Kind of Transrectal Biopsies: 3 by IRM-echography Image Fusion and 12 Systematized Guided Echographies.; ODM derived from: https://clinicaltrials.gov/show/NCT02050542

Link

https://clinicaltrials.gov/show/NCT02050542

Trefwoorden

  1. 17-01-19 17-01-19 -
  2. 11-02-20 11-02-20 - Christian Arras
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

17 januari 2019

DOI

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Licentie

Creative Commons BY-NC 3.0

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Eligibility Prostate Cancer Based on a Rise of the PSA > 4 ng / mL. NCT02050542

Eligibility Prostate Cancer Based on a Rise of the PSA > 4 ng / mL. NCT02050542

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient from 45 to 75 years old;
Beschrijving

ID.1

Datatype

boolean

serum level of psa > 4,0 ng / ml;
Beschrijving

ID.2

Datatype

boolean

multiparametric prostate irm, performed before inclusion and which confirm the diagnosis of suspected target;
Beschrijving

ID.3

Datatype

boolean

no opposition of the patient notified in the medical record
Beschrijving

ID.4

Datatype

boolean

patient member in a national insurance scheme.
Beschrijving

ID.5

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
previous prostate biopsy;
Beschrijving

ID.6

Datatype

boolean

suspicious digital rectal examination;
Beschrijving

ID.7

Datatype

boolean

serum psa > 20,0 ng / ml;
Beschrijving

ID.8

Datatype

boolean

treatment with 5 alpha reductase inhibitor during the last 3 months;
Beschrijving

ID.9

Datatype

boolean

untreated urinary infection
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Prostate Cancer Based on a Rise of the PSA > 4 ng / mL. NCT02050542

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
patient from 45 to 75 years old;
boolean
ID.2
Item
serum level of psa > 4,0 ng / ml;
boolean
ID.3
Item
multiparametric prostate irm, performed before inclusion and which confirm the diagnosis of suspected target;
boolean
ID.4
Item
no opposition of the patient notified in the medical record
boolean
ID.5
Item
patient member in a national insurance scheme.
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
previous prostate biopsy;
boolean
ID.7
Item
suspicious digital rectal examination;
boolean
ID.8
Item
serum psa > 20,0 ng / ml;
boolean
ID.9
Item
treatment with 5 alpha reductase inhibitor during the last 3 months;
boolean
ID.10
Item
untreated urinary infection
boolean

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