ID

31598

Descrizione

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

collegamento

https://clinicaltrials.gov/show/NCT00801996

Keywords

  1. 10/09/18 10/09/18 -
Titolare del copyright

See clinicaltrials.gov

Caricato su

10 settembre 2018

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0

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Eligibility Prostate Cancer NCT00801996

Eligibility Prostate Cancer NCT00801996

Criteria
Descrizione

Criteria

Inclusion Criteria
Descrizione

Inclusion Criteria

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

Informed Consent

Tipo di dati

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)
Descrizione

Age

Tipo di dati

boolean

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

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

Tipo di dati

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
Descrizione

Exclusion Criteria

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

Family history of prostate cancer

Tipo di dati

boolean

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

Good health Lacking

Tipo di dati

boolean

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

Eligibility Criteria Prostate Cohort

Tipo di dati

boolean

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

Inclusion Criteria

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

Informed Consent

Tipo di dati

boolean

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

Gender | Age

Tipo di dati

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.
Descrizione

Individuals Qatar | Ancestors Qatar

Tipo di dati

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
Descrizione

TRUS - Transrectal ultrasonography

Tipo di dati

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
Descrizione

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

Tipo di dati

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
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
• patient refuses consent
Descrizione

Informed Consent Refused

Tipo di dati

boolean

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

Similar models

Eligibility Prostate Cancer NCT00801996

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
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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