ID

31632

Descripción

Transrectal Ultrasound Imaging of the Prostate Gland and Neurovascular Bundles During Robot-Assisted Laparoscopic Radical Prostatectomy; ODM derived from: https://clinicaltrials.gov/show/NCT00952666

Link

https://clinicaltrials.gov/show/NCT00952666

Palabras clave

  1. 14/9/18 14/9/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

14 de septiembre de 2018

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Prostate Cancer NCT00952666

Eligibility Prostate Cancer NCT00952666

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients scheduled for a laparoscopic radical prostatectomy operation
Descripción

Laparoscopic Prostatectomy Radical Scheduled

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2986522
UMLS CUI [1,2]
C0439807
UMLS CUI [1,3]
C0205539
patients must be between the ages of 35 and 75
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
patients must not have one of the above listed exclusion criteria
Descripción

Exclusion Criteria Mismatch

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C1881865
patients must be able to understand and willing to adhere to the study protocol
Descripción

Protocol Compliance

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0525058
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients less than 35 years of age and over 75 years of age
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
patients with previous rectal surgery
Descripción

Rectal surgery

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2066000
patients with anal stenosis that prevents the trus probe insertion
Descripción

Anal stenosis Preventing TRUS Insertion of probe

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0262374
UMLS CUI [1,2]
C1292733
UMLS CUI [1,3]
C0373345
UMLS CUI [1,4]
C0419358
patients with extensive abdominal surgery
Descripción

Abdominal surgery Extensive

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0198482
UMLS CUI [1,2]
C0205231
patients with inadequate bowel prep
Descripción

Inadequate bowel preparation

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1446338
patients who are unwilling or unable to sign informed consent
Descripción

Informed Consent Unwilling | Informed Consent Unable

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0558080
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C1299582
patients on anticoagulation medication (e.g., coumadin, lovenox, or heparin)
Descripción

Anticoagulants | Coumadin | Lovenox | Heparin

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0003280
UMLS CUI [2]
C0699129
UMLS CUI [3]
C0728963
UMLS CUI [4]
C0019134

Similar models

Eligibility Prostate Cancer NCT00952666

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Laparoscopic Prostatectomy Radical Scheduled
Item
patients scheduled for a laparoscopic radical prostatectomy operation
boolean
C2986522 (UMLS CUI [1,1])
C0439807 (UMLS CUI [1,2])
C0205539 (UMLS CUI [1,3])
Age
Item
patients must be between the ages of 35 and 75
boolean
C0001779 (UMLS CUI [1])
Exclusion Criteria Mismatch
Item
patients must not have one of the above listed exclusion criteria
boolean
C0680251 (UMLS CUI [1,1])
C1881865 (UMLS CUI [1,2])
Protocol Compliance
Item
patients must be able to understand and willing to adhere to the study protocol
boolean
C0525058 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Age
Item
patients less than 35 years of age and over 75 years of age
boolean
C0001779 (UMLS CUI [1])
Rectal surgery
Item
patients with previous rectal surgery
boolean
C2066000 (UMLS CUI [1])
Anal stenosis Preventing TRUS Insertion of probe
Item
patients with anal stenosis that prevents the trus probe insertion
boolean
C0262374 (UMLS CUI [1,1])
C1292733 (UMLS CUI [1,2])
C0373345 (UMLS CUI [1,3])
C0419358 (UMLS CUI [1,4])
Abdominal surgery Extensive
Item
patients with extensive abdominal surgery
boolean
C0198482 (UMLS CUI [1,1])
C0205231 (UMLS CUI [1,2])
Inadequate bowel preparation
Item
patients with inadequate bowel prep
boolean
C1446338 (UMLS CUI [1])
Informed Consent Unwilling | Informed Consent Unable
Item
patients who are unwilling or unable to sign informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
Anticoagulants | Coumadin | Lovenox | Heparin
Item
patients on anticoagulation medication (e.g., coumadin, lovenox, or heparin)
boolean
C0003280 (UMLS CUI [1])
C0699129 (UMLS CUI [2])
C0728963 (UMLS CUI [3])
C0019134 (UMLS CUI [4])

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