ID

34475

Descrição

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

Link

https://clinicaltrials.gov/show/NCT01347320

Palavras-chave

  1. 17/01/2019 17/01/2019 -
  2. 27/05/2019 27/05/2019 -
  3. 29/05/2019 29/05/2019 - Sarah Riepenhausen
Titular dos direitos

see on clinicaltrials.gov

Transferido a

17 de janeiro de 2019

DOI

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Licença

Creative Commons BY-NC 3.0

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Eligibility Prostate Cancer NCT01347320

Eligibility Prostate Cancer NCT01347320

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
all patients suitable for surgery.
Descrição

ID.1

Tipo de dados

boolean

positive biopsy (gleason grade >3).
Descrição

ID.2

Tipo de dados

boolean

informed consent.
Descrição

ID.3

Tipo de dados

boolean

Exclusion Criteria
Descrição

Exclusion Criteria

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

ID.4

Tipo de dados

boolean

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

ID.5

Tipo de dados

boolean

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

ID.6

Tipo de dados

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).
Descrição

ID.7

Tipo de dados

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.
Descrição

ID.8

Tipo de dados

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.
Descrição

ID.9

Tipo de dados

boolean

Similar models

Eligibility Prostate Cancer NCT01347320

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
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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