ID

31598

Beschrijving

Prostate Cancer - Qatar; ODM derived from: https://clinicaltrials.gov/show/NCT00801996

Link

https://clinicaltrials.gov/show/NCT00801996

Trefwoorden

  1. 10-09-18 10-09-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

10 september 2018

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Prostate Cancer NCT00801996

Eligibility Prostate Cancer NCT00801996

Criteria
Beschrijving

Criteria

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
all study subjects should be able to provide informed consent
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
males or females ages 40 years or older (see section a8 for the rationale for the inclusion of females)
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
individuals of arab descent from qatari peninsula without any personal or family history of prostate cancer
Beschrijving

Arab ethnic group Qatar | Medical History Prostate carcinoma Absent | Family history of prostate cancer Absent

Datatype

boolean

Alias
UMLS CUI [1,1]
C0282540
UMLS CUI [1,2]
C0034366
UMLS CUI [2,1]
C0262926
UMLS CUI [2,2]
C0600139
UMLS CUI [2,3]
C0332197
UMLS CUI [3,1]
C1532320
UMLS CUI [3,2]
C0332197
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
individuals with family history of prostate cancer
Beschrijving

Family history of prostate cancer

Datatype

boolean

Alias
UMLS CUI [1]
C1532320
individuals not deemed in good overall health by the investigator will not be accepted into the study
Beschrijving

Good health Lacking

Datatype

boolean

Alias
UMLS CUI [1,1]
C3813622
UMLS CUI [1,2]
C0332268
inclusion/exclusion criteria for prostate cohort
Beschrijving

Eligibility Criteria Prostate Cohort

Datatype

boolean

Alias
UMLS CUI [1,1]
C1516637
UMLS CUI [1,2]
C0033572
UMLS CUI [1,3]
C0599755
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
all study subjects should be able to provide informed consent
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
males ages 40 years or older
Beschrijving

Gender | Age

Datatype

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
individuals from the qatari peninsula whose ancestors up to three generations back were natives of qatar.
Beschrijving

Individuals Qatar | Ancestors Qatar

Datatype

boolean

Alias
UMLS CUI [1,1]
C0027361
UMLS CUI [1,2]
C0034366
UMLS CUI [2,1]
C0870134
UMLS CUI [2,2]
C0034366
individuals undergoing trans rectal ultrasound (trus) biopsy as dictated by their standard clinical care
Beschrijving

TRUS - Transrectal ultrasonography

Datatype

boolean

Alias
UMLS CUI [1]
C2960324
ultrasound or digital rectal examination consistent with prostate disease or a level of psa (prostatic specific antigen) greater than 3.0
Beschrijving

Ultrasonography Consistent with Prostatic Disease | Digital Rectal Examination Consistent with Prostatic Disease | Prostate specific antigen measurement

Datatype

boolean

Alias
UMLS CUI [1,1]
C0041618
UMLS CUI [1,2]
C0332290
UMLS CUI [1,3]
C0033575
UMLS CUI [2,1]
C1384593
UMLS CUI [2,2]
C0332290
UMLS CUI [2,3]
C0033575
UMLS CUI [3]
C0201544
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
• patient refuses consent
Beschrijving

Informed Consent Refused

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1705116

Similar models

Eligibility Prostate Cancer NCT00801996

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Item Group
C1512693 (UMLS CUI)
Informed Consent
Item
all study subjects should be able to provide informed consent
boolean
C0021430 (UMLS CUI [1])
Age
Item
males or females ages 40 years or older (see section a8 for the rationale for the inclusion of females)
boolean
C0001779 (UMLS CUI [1])
Arab ethnic group Qatar | Medical History Prostate carcinoma Absent | Family history of prostate cancer Absent
Item
individuals of arab descent from qatari peninsula without any personal or family history of prostate cancer
boolean
C0282540 (UMLS CUI [1,1])
C0034366 (UMLS CUI [1,2])
C0262926 (UMLS CUI [2,1])
C0600139 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
C1532320 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
Item Group
C0680251 (UMLS CUI)
Family history of prostate cancer
Item
individuals with family history of prostate cancer
boolean
C1532320 (UMLS CUI [1])
Good health Lacking
Item
individuals not deemed in good overall health by the investigator will not be accepted into the study
boolean
C3813622 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
Eligibility Criteria Prostate Cohort
Item
inclusion/exclusion criteria for prostate cohort
boolean
C1516637 (UMLS CUI [1,1])
C0033572 (UMLS CUI [1,2])
C0599755 (UMLS CUI [1,3])
Item Group
C1512693 (UMLS CUI)
Informed Consent
Item
all study subjects should be able to provide informed consent
boolean
C0021430 (UMLS CUI [1])
Gender | Age
Item
males ages 40 years or older
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Individuals Qatar | Ancestors Qatar
Item
individuals from the qatari peninsula whose ancestors up to three generations back were natives of qatar.
boolean
C0027361 (UMLS CUI [1,1])
C0034366 (UMLS CUI [1,2])
C0870134 (UMLS CUI [2,1])
C0034366 (UMLS CUI [2,2])
TRUS - Transrectal ultrasonography
Item
individuals undergoing trans rectal ultrasound (trus) biopsy as dictated by their standard clinical care
boolean
C2960324 (UMLS CUI [1])
Ultrasonography Consistent with Prostatic Disease | Digital Rectal Examination Consistent with Prostatic Disease | Prostate specific antigen measurement
Item
ultrasound or digital rectal examination consistent with prostate disease or a level of psa (prostatic specific antigen) greater than 3.0
boolean
C0041618 (UMLS CUI [1,1])
C0332290 (UMLS CUI [1,2])
C0033575 (UMLS CUI [1,3])
C1384593 (UMLS CUI [2,1])
C0332290 (UMLS CUI [2,2])
C0033575 (UMLS CUI [2,3])
C0201544 (UMLS CUI [3])
Item Group
C0680251 (UMLS CUI)
Informed Consent Refused
Item
• patient refuses consent
boolean
C0021430 (UMLS CUI [1,1])
C1705116 (UMLS CUI [1,2])

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