Information:
Fel:
ID
36572
Beskrivning
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
Länk
https://clinicaltrials.gov/show/NCT01409876
Nyckelord
Versioner (2)
- 2019-01-17 2019-01-17 -
- 2019-05-22 2019-05-22 -
Rättsinnehavare
University Hospital Erlangen
Uppladdad den
22 maj 2019
DOI
För en begäran logga in.
Licens
Creative Commons BY-NC 3.0
Modellkommentarer :
Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.
Itemgroup-kommentar för :
Item-kommentar för :
Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.
HistoScanning-based Brachytherapy in Prostate Cancer NCT01409876
Similar models
Eligibility Criteria
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
histologically proven prostate cancer
Item
histologically proven prostate cancer
boolean
C0600139 (UMLS CUI [1,1])
C0449575 (UMLS CUI [1,2])
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])
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])
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])
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])
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])
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])
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])
C0005778 (UMLS CUI [1,2])
C0587081 (UMLS CUI [1,3])