ID

34474

Description

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

Keywords

  1. 1/17/19 1/17/19 -
  2. 5/27/19 5/27/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 17, 2019

DOI

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License

Creative Commons BY-NC 3.0

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Eligibility Prostate Cancer NCT01191099

Eligibility Prostate Cancer NCT01191099

Inclusion Criteria
Description

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
Description

ID.1

Data type

boolean

written informed consent
Description

ID.2

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
metastatic prostate cancer
Description

ID.3

Data type

boolean

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

ID.4

Data type

boolean

severe heart or lung disease
Description

ID.5

Data type

boolean

severe liver or kidney dysfunction
Description

ID.6

Data type

boolean

severe stridor
Description

ID.7

Data type

boolean

distant metastases
Description

ID.8

Data type

boolean

concurrent treatment for other malignant disease
Description

ID.9

Data type

boolean

prior hormonal therapy or radiotherapy
Description

ID.10

Data type

boolean

Similar models

Eligibility Prostate Cancer NCT01191099

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
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
ID.2
Item
written informed consent
boolean
Item Group
C0680251 (UMLS CUI)
ID.3
Item
metastatic prostate cancer
boolean
ID.4
Item
contraindications to the class of investigational product under study, e.g. known hypersensitivity or allergy to the investigational product
boolean
ID.5
Item
severe heart or lung disease
boolean
ID.6
Item
severe liver or kidney dysfunction
boolean
ID.7
Item
severe stridor
boolean
ID.8
Item
distant metastases
boolean
ID.9
Item
concurrent treatment for other malignant disease
boolean
ID.10
Item
prior hormonal therapy or radiotherapy
boolean

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