ID

36640

Beschrijving

Comprehensive Analysis of Hypoxia in Prostate Cancer: Diagnostic Markers and Prognostic Significance; ODM derived from: https://clinicaltrials.gov/show/NCT01191099

Link

https://clinicaltrials.gov/show/NCT01191099

Trefwoorden

Versies (2)
  1. 17-01-19 17-01-19 -
  2. 27-05-19 27-05-19 -
Houder van rechten

University of Zurich

Geüploaded op

27 mei 2019

DOI

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Licentie

Creative Commons BY-NC 3.0
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Hypoxia in Prostate Cancer NCT01191099

Engels

Eligibility

1 Formulieren  
  1. StudyEvent: Eligibility
    1. Eligibility
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with biopsy-proven adenocarcinoma of the prostate who are to be treated with radical prostatectomy at the department of urology, university hospital of Zurich
Beschrijving

biopsy-proven adenocarcinoma of the prostate, to be treated with radical prostatectomy at study site

Datatype

boolean

Alias
UMLS CUI [1,1]
C0005558
UMLS CUI [1,2]
C0750484
UMLS CUI [1,3]
C0007112
UMLS CUI [2,1]
C0194810
UMLS CUI [2,2]
C1301732
UMLS CUI [2,3]
C2825164
written informed consent
Beschrijving

Informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
metastatic prostate cancer
Beschrijving

metastatic prostate cancer

Datatype

boolean

Alias
UMLS CUI [1]
C0936223
contraindications to the class of investigational product under study, e.g. known hypersensitivity or allergy to the investigational product
Beschrijving

contraindications to the class of investigational product under study, e.g. known hypersensitivity or allergy to the investigational product

Datatype

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C2983595
UMLS CUI [2,1]
C0205309
UMLS CUI [2,2]
C0020517
UMLS CUI [2,3]
C0304229
UMLS CUI [3,1]
C0205309
UMLS CUI [3,2]
C0013182
UMLS CUI [3,3]
C0304229
severe heart or lung disease
Beschrijving

severe heart or lung disease

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018799
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C0024115
UMLS CUI [2,2]
C0205082
severe liver or kidney dysfunction
Beschrijving

severe liver or kidney dysfunction

Datatype

boolean

Alias
UMLS CUI [1,1]
C0086565
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C0205082
UMLS CUI [2,2]
C3279454
severe stridor
Beschrijving

severe stridor

Datatype

boolean

Alias
UMLS CUI [1,1]
C0038450
UMLS CUI [1,2]
C0205082
distant metastases
Beschrijving

distant metastases

Datatype

boolean

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0443203
concurrent treatment for other malignant disease
Beschrijving

concurrent treatment for other malignant disease

Datatype

boolean

Alias
UMLS CUI [1,1]
C0521116
UMLS CUI [1,2]
C0087111
UMLS CUI [1,3]
C0205394
UMLS CUI [1,4]
C0006826
prior hormonal therapy or radiotherapy
Beschrijving

prior hormonal therapy or radiotherapy

Datatype

boolean

Alias
UMLS CUI [1]
C1514460
UMLS CUI [2]
C0279134
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Similar models

Eligibility

1 Formulieren
  1. StudyEvent: Eligibility
    1. Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
biopsy-proven adenocarcinoma of the prostate, to be treated with radical prostatectomy at study site
Item
patients with biopsy-proven adenocarcinoma of the prostate who are to be treated with radical prostatectomy at the department of urology, university hospital of Zurich
boolean
C0005558 (UMLS CUI [1,1])
C0750484 (UMLS CUI [1,2])
C0007112 (UMLS CUI [1,3])
C0194810 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
C2825164 (UMLS CUI [2,3])
Informed consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
metastatic prostate cancer
Item
metastatic prostate cancer
boolean
C0936223 (UMLS CUI [1])
contraindications to the class of investigational product under study, e.g. known hypersensitivity or allergy to the investigational product
Item
contraindications to the class of investigational product under study, e.g. known hypersensitivity or allergy to the investigational product
boolean
C1301624 (UMLS CUI [1,1])
C2983595 (UMLS CUI [1,2])
C0205309 (UMLS CUI [2,1])
C0020517 (UMLS CUI [2,2])
C0304229 (UMLS CUI [2,3])
C0205309 (UMLS CUI [3,1])
C0013182 (UMLS CUI [3,2])
C0304229 (UMLS CUI [3,3])
severe heart or lung disease
Item
severe heart or lung disease
boolean
C0018799 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0024115 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
severe liver or kidney dysfunction
Item
severe liver or kidney dysfunction
boolean
C0086565 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0205082 (UMLS CUI [2,1])
C3279454 (UMLS CUI [2,2])
severe stridor
Item
severe stridor
boolean
C0038450 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
distant metastases
Item
distant metastases
boolean
C0027627 (UMLS CUI [1,1])
C0443203 (UMLS CUI [1,2])
concurrent treatment for other malignant disease
Item
concurrent treatment for other malignant disease
boolean
C0521116 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C0006826 (UMLS CUI [1,4])
prior hormonal therapy or radiotherapy
Item
prior hormonal therapy or radiotherapy
boolean
C1514460 (UMLS CUI [1])
C0279134 (UMLS CUI [2])
Terug naar het begin van de pagina 

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