ID

34477

Description

HistScanning- Based PDR Brachytherapy in Prostate Cancer HistoScanning- Based Interstitial PDR Brachytherapy; ODM derived from: https://clinicaltrials.gov/show/NCT01409876

Link

https://clinicaltrials.gov/show/NCT01409876

Keywords

  1. 1/17/19 1/17/19 -
  2. 5/22/19 5/22/19 -
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 NCT01409876

Eligibility Prostate Cancer NCT01409876

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically proven prostate cancer
Description

ID.1

Data type

boolean

all ct1-3 carcinomas independent of grading and psa value
Description

ID.2

Data type

boolean

prostate volume< 70cc
Description

ID.3

Data type

boolean

no distant metastases
Description

ID.4

Data type

boolean

karnofsky > 60
Description

ID.5

Data type

boolean

written informed consent from the patient regarding study participation
Description

ID.6

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
all patients who do not meet the inclusion criteria
Description

ID.7

Data type

boolean

t4 carcinomas
Description

ID.8

Data type

boolean

proven metastases n+ and/or m1
Description

ID.9

Data type

boolean

epidural or general anaesthesia not possible
Description

ID.10

Data type

boolean

pathological clotting parameters
Description

ID.11

Data type

boolean

Similar models

Eligibility Prostate Cancer NCT01409876

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
histologically proven prostate cancer
boolean
ID.2
Item
all ct1-3 carcinomas independent of grading and psa value
boolean
ID.3
Item
prostate volume< 70cc
boolean
ID.4
Item
no distant metastases
boolean
ID.5
Item
karnofsky > 60
boolean
ID.6
Item
written informed consent from the patient regarding study participation
boolean
Item Group
C0680251 (UMLS CUI)
ID.7
Item
all patients who do not meet the inclusion criteria
boolean
ID.8
Item
t4 carcinomas
boolean
ID.9
Item
proven metastases n+ and/or m1
boolean
ID.10
Item
epidural or general anaesthesia not possible
boolean
ID.11
Item
pathological clotting parameters
boolean

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