ID

31632

Description

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

Keywords

Versions (1)
  1. 9/14/18 9/14/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

September 14, 2018

DOI

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License

Creative Commons BY 4.0
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Eligibility Prostate Cancer NCT00952666

English

Eligibility Prostate Cancer NCT00952666

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

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

Laparoscopic Prostatectomy Radical Scheduled

Data type

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
Description

Age

Data type

boolean

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

Exclusion Criteria Mismatch

Data type

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
Description

Protocol Compliance

Data type

boolean

Alias
UMLS CUI [1]
C0525058
Exclusion Criteria
Description

Exclusion Criteria

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

Age

Data type

boolean

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

Rectal surgery

Data type

boolean

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

Anal stenosis Preventing TRUS Insertion of probe

Data type

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
Description

Abdominal surgery Extensive

Data type

boolean

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

Inadequate bowel preparation

Data type

boolean

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

Informed Consent Unwilling | Informed Consent Unable

Data type

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)
Description

Anticoagulants | Coumadin | Lovenox | Heparin

Data type

boolean

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

Eligibility Prostate Cancer NCT00952666

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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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