ID

34475

Beschrijving

Preoperative Magnetic Resonance (MR) Imaging of Prostate Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01347320

Link

https://clinicaltrials.gov/show/NCT01347320

Trefwoorden

  1. 17-01-19 17-01-19 -
  2. 27-05-19 27-05-19 -
  3. 29-05-19 29-05-19 - Sarah Riepenhausen
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

17 januari 2019

DOI

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Licentie

Creative Commons BY-NC 3.0

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Eligibility Prostate Cancer NCT01347320

Eligibility Prostate Cancer NCT01347320

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
all patients suitable for surgery.
Beschrijving

ID.1

Datatype

boolean

positive biopsy (gleason grade >3).
Beschrijving

ID.2

Datatype

boolean

informed consent.
Beschrijving

ID.3

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who do not sign the consent paper for any reason or do not accept the study premises.
Beschrijving

ID.4

Datatype

boolean

patents who want to withdraw for any reason during the study.
Beschrijving

ID.5

Datatype

boolean

patients with contraindications to mri (pacemaker, claustrophobia etc) and/or surgery.
Beschrijving

ID.6

Datatype

boolean

patients who have undergone a high quality mri examination of the prostate at another radiological center. in this situation the mr examination is evaluated together with the surgeon but the patient is not included in the study. (in case of a low quality examinations, we will disregard the findings, and include the patient).
Beschrijving

ID.7

Datatype

boolean

if the surgeon finds it unacceptable to perform ralp without mri, because of various reasons (eg. patient demand, too high risk etc) the patient will not be included in the study.
Beschrijving

ID.8

Datatype

boolean

if preoperative mri reveals extensive tumor invasion into adjacent organ (t4) or skeletal metastases (m1), as these cancer stadiums do not benefit from ralp.
Beschrijving

ID.9

Datatype

boolean

Similar models

Eligibility Prostate Cancer NCT01347320

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
all patients suitable for surgery.
boolean
ID.2
Item
positive biopsy (gleason grade >3).
boolean
ID.3
Item
informed consent.
boolean
Item Group
C0680251 (UMLS CUI)
ID.4
Item
patients who do not sign the consent paper for any reason or do not accept the study premises.
boolean
ID.5
Item
patents who want to withdraw for any reason during the study.
boolean
ID.6
Item
patients with contraindications to mri (pacemaker, claustrophobia etc) and/or surgery.
boolean
ID.7
Item
patients who have undergone a high quality mri examination of the prostate at another radiological center. in this situation the mr examination is evaluated together with the surgeon but the patient is not included in the study. (in case of a low quality examinations, we will disregard the findings, and include the patient).
boolean
ID.8
Item
if the surgeon finds it unacceptable to perform ralp without mri, because of various reasons (eg. patient demand, too high risk etc) the patient will not be included in the study.
boolean
ID.9
Item
if preoperative mri reveals extensive tumor invasion into adjacent organ (t4) or skeletal metastases (m1), as these cancer stadiums do not benefit from ralp.
boolean

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