ID

31632

Beschrijving

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

Trefwoorden

  1. 14-09-18 14-09-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

14 september 2018

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Prostate Cancer NCT00952666

Eligibility Prostate Cancer NCT00952666

Inclusion Criteria
Beschrijving

Inclusion Criteria

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

Laparoscopic Prostatectomy Radical Scheduled

Datatype

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
Beschrijving

Age

Datatype

boolean

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

Exclusion Criteria Mismatch

Datatype

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
Beschrijving

Protocol Compliance

Datatype

boolean

Alias
UMLS CUI [1]
C0525058
Exclusion Criteria
Beschrijving

Exclusion Criteria

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

Age

Datatype

boolean

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

Rectal surgery

Datatype

boolean

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

Anal stenosis Preventing TRUS Insertion of probe

Datatype

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
Beschrijving

Abdominal surgery Extensive

Datatype

boolean

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

Inadequate bowel preparation

Datatype

boolean

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

Informed Consent Unwilling | Informed Consent Unable

Datatype

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)
Beschrijving

Anticoagulants | Coumadin | Lovenox | Heparin

Datatype

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
Type
Description | Question | Decode (Coded Value)
Datatype
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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