ID

36572

Beschrijving

Phase II trial looking at the feasibility of HistoScanning-based dose-painting image-guided interstitial brachytherapy in non-metastatic prostate cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01409876

Link

https://clinicaltrials.gov/show/NCT01409876

Trefwoorden

  1. 17-01-19 17-01-19 -
  2. 22-05-19 22-05-19 -
Houder van rechten

University Hospital Erlangen

Geüploaded op

22 mei 2019

DOI

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Licentie

Creative Commons BY-NC 3.0

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HistoScanning-based Brachytherapy in Prostate Cancer NCT01409876

Eligibility Criteria

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

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically proven prostate cancer
Beschrijving

histologically proven prostate cancer

Datatype

boolean

Alias
UMLS CUI [1,1]
C0600139
UMLS CUI [1,2]
C0449575
all cT1-3 carcinomas independent of grading and psa value
Beschrijving

cT staging

Datatype

boolean

Alias
UMLS CUI [1,1]
C3258246
UMLS CUI [1,2]
C0475455
UMLS CUI [2]
C0919553
UMLS CUI [3]
C0201544
prostate volume< 70cc
Beschrijving

Prostate volume

Datatype

boolean

Alias
UMLS CUI [1]
C1441416
no distant metastases
Beschrijving

no distant metastases

Datatype

boolean

Alias
UMLS CUI [1,1]
C0332197
UMLS CUI [1,2]
C1302548
Karnofsky > 60
Beschrijving

Karnofsky status

Datatype

boolean

Alias
UMLS CUI [1]
C0206065
written informed consent from the patient regarding study participation
Beschrijving

Informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

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

Not meeting inclusion criteria

Datatype

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0231175
T4 carcinomas
Beschrijving

T staging

Datatype

boolean

Alias
UMLS CUI [1]
C0475455
proven metastases N+ and/or M1
Beschrijving

proven metastases

Datatype

boolean

Alias
UMLS CUI [1,1]
C0750484
UMLS CUI [1,2]
C0456532
UMLS CUI [2,1]
C0750484
UMLS CUI [2,2]
C3258247
epidural or general anaesthesia not possible
Beschrijving

epidural or general anaesthesia not possible

Datatype

boolean

Alias
UMLS CUI [1,1]
C0002913
UMLS CUI [1,2]
C1301624
UMLS CUI [2,1]
C0002915
UMLS CUI [2,2]
C1301624
pathological clotting parameters
Beschrijving

pathological clotting parameters

Datatype

boolean

Alias
UMLS CUI [1,1]
C1521733
UMLS CUI [1,2]
C0005778
UMLS CUI [1,3]
C0587081

Similar models

Eligibility Criteria

  1. StudyEvent: Eligibility
    1. Eligibility Criteria
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
histologically proven prostate cancer
Item
histologically proven prostate cancer
boolean
C0600139 (UMLS CUI [1,1])
C0449575 (UMLS CUI [1,2])
cT staging
Item
all cT1-3 carcinomas independent of grading and psa value
boolean
C3258246 (UMLS CUI [1,1])
C0475455 (UMLS CUI [1,2])
C0919553 (UMLS CUI [2])
C0201544 (UMLS CUI [3])
Prostate volume
Item
prostate volume< 70cc
boolean
C1441416 (UMLS CUI [1])
no distant metastases
Item
no distant metastases
boolean
C0332197 (UMLS CUI [1,1])
C1302548 (UMLS CUI [1,2])
Karnofsky status
Item
Karnofsky > 60
boolean
C0206065 (UMLS CUI [1])
Informed consent
Item
written informed consent from the patient regarding study participation
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Not meeting inclusion criteria
Item
all patients who do not meet the inclusion criteria
boolean
C1512693 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
T staging
Item
T4 carcinomas
boolean
C0475455 (UMLS CUI [1])
proven metastases
Item
proven metastases N+ and/or M1
boolean
C0750484 (UMLS CUI [1,1])
C0456532 (UMLS CUI [1,2])
C0750484 (UMLS CUI [2,1])
C3258247 (UMLS CUI [2,2])
epidural or general anaesthesia not possible
Item
epidural or general anaesthesia not possible
boolean
C0002913 (UMLS CUI [1,1])
C1301624 (UMLS CUI [1,2])
C0002915 (UMLS CUI [2,1])
C1301624 (UMLS CUI [2,2])
pathological clotting parameters
Item
pathological clotting parameters
boolean
C1521733 (UMLS CUI [1,1])
C0005778 (UMLS CUI [1,2])
C0587081 (UMLS CUI [1,3])

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