ID

13107

Beschreibung

Screening for Prostate Cancer in Older Patients (PLCO Screening Trial); ODM derived from: https://clinicaltrials.gov/show/NCT00002540

Link

https://clinicaltrials.gov/show/NCT00002540

Stichworte

  1. 17.01.16 17.01.16 -
Hochgeladen am

17. Januar 2016

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Prostate Carcinoma NCT00002540

Eligibility Prostate Carcinoma NCT00002540

Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
men who at the time of randomization are less than 55 or greater than or equal to 75 years of age
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
individuals undergoing treatment for cancer at this time, excluding basal-cell and squamous-cell skin cancer
Beschreibung

malignancies, treatment for cancer, exceptions

Datentyp

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2]
C0920425
UMLS CUI [3]
C0007117
UMLS CUI [4]
C0553723
individuals with known prior cancer of the colon, rectum, lung, prostate
Beschreibung

cancer of the colon, rectum, lung, prostate

Datentyp

boolean

Alias
UMLS CUI [1]
C0699790
UMLS CUI [2]
C0007113
UMLS CUI [3]
C0242379
UMLS CUI [4]
C0600139
this includes primary or metastatic plco cancers
Beschreibung

primary or metastatic plco cancers

Datentyp

boolean

Alias
UMLS CUI [1]
C1514515
UMLS CUI [2]
C0699790
UMLS CUI [3]
C0242379
UMLS CUI [4]
C0600139
UMLS CUI [5]
C0029925
individuals with previous surgical removal of the entire colon, one lung, or the entire prostate
Beschreibung

surgical removal of the entire colon, one lung, or the entire prostate

Datentyp

boolean

Alias
UMLS CUI [1]
C0038894
UMLS CUI [2,1]
C1408858
UMLS CUI [2,2]
C0009368
UMLS CUI [3,1]
C1408858
UMLS CUI [3,2]
C0024109
UMLS CUI [4,1]
C1408858
UMLS CUI [4,2]
C0033572
individuals who are participating in another cancer screening or cancer primary prevention trial
Beschreibung

participating in another trial

Datentyp

boolean

Alias
UMLS CUI [1]
C2348568
males who have taken proscar/propecia/finasteride in the past 6 months
Beschreibung

proscar, propecia, finasteride

Datentyp

boolean

Alias
UMLS CUI [1]
C0678149
UMLS CUI [2]
C0722858
UMLS CUI [3]
C0060389
note: individuals who are already enrolled in the trial when their physician prescribes finasteride are not prevented from taking this medication. as a result, these participants will continue to be screened and followed just as those participants who are not on finasteride.
Beschreibung

finasteride additional information

Datentyp

boolean

Alias
UMLS CUI [1]
C0060389
note: men who are taking tamoxifen are not excluded from any part of the plco screening trial.
Beschreibung

tamoxifen

Datentyp

boolean

Alias
UMLS CUI [1]
C0039286
individuals who are unwilling or unable to sign the informed consent form
Beschreibung

informed consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
males who have had more than one psa blood test in the past three years
Beschreibung

psa blood test

Datentyp

boolean

Alias
UMLS CUI [1]
C0138741
individuals who have had a colonoscopy, sigmoidoscopy, or barium enema in the past three years
Beschreibung

colonoscopy, sigmoidoscopy, or barium enema

Datentyp

boolean

Alias
UMLS CUI [1]
C0009378
UMLS CUI [2]
C0037075
UMLS CUI [3]
C0203075

Ähnliche Modelle

Eligibility Prostate Carcinoma NCT00002540

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C0680251 (UMLS CUI)
Age
Item
men who at the time of randomization are less than 55 or greater than or equal to 75 years of age
boolean
C0001779 (UMLS CUI [1])
malignancies, treatment for cancer, exceptions
Item
individuals undergoing treatment for cancer at this time, excluding basal-cell and squamous-cell skin cancer
boolean
C0006826 (UMLS CUI [1])
C0920425 (UMLS CUI [2])
C0007117 (UMLS CUI [3])
C0553723 (UMLS CUI [4])
cancer of the colon, rectum, lung, prostate
Item
individuals with known prior cancer of the colon, rectum, lung, prostate
boolean
C0699790 (UMLS CUI [1])
C0007113 (UMLS CUI [2])
C0242379 (UMLS CUI [3])
C0600139 (UMLS CUI [4])
primary or metastatic plco cancers
Item
this includes primary or metastatic plco cancers
boolean
C1514515 (UMLS CUI [1])
C0699790 (UMLS CUI [2])
C0242379 (UMLS CUI [3])
C0600139 (UMLS CUI [4])
C0029925 (UMLS CUI [5])
surgical removal of the entire colon, one lung, or the entire prostate
Item
individuals with previous surgical removal of the entire colon, one lung, or the entire prostate
boolean
C0038894 (UMLS CUI [1])
C1408858 (UMLS CUI [2,1])
C0009368 (UMLS CUI [2,2])
C1408858 (UMLS CUI [3,1])
C0024109 (UMLS CUI [3,2])
C1408858 (UMLS CUI [4,1])
C0033572 (UMLS CUI [4,2])
participating in another trial
Item
individuals who are participating in another cancer screening or cancer primary prevention trial
boolean
C2348568 (UMLS CUI [1])
proscar, propecia, finasteride
Item
males who have taken proscar/propecia/finasteride in the past 6 months
boolean
C0678149 (UMLS CUI [1])
C0722858 (UMLS CUI [2])
C0060389 (UMLS CUI [3])
finasteride additional information
Item
note: individuals who are already enrolled in the trial when their physician prescribes finasteride are not prevented from taking this medication. as a result, these participants will continue to be screened and followed just as those participants who are not on finasteride.
boolean
C0060389 (UMLS CUI [1])
tamoxifen
Item
note: men who are taking tamoxifen are not excluded from any part of the plco screening trial.
boolean
C0039286 (UMLS CUI [1])
informed consent
Item
individuals who are unwilling or unable to sign the informed consent form
boolean
C0021430 (UMLS CUI [1])
psa blood test
Item
males who have had more than one psa blood test in the past three years
boolean
C0138741 (UMLS CUI [1])
colonoscopy, sigmoidoscopy, or barium enema
Item
individuals who have had a colonoscopy, sigmoidoscopy, or barium enema in the past three years
boolean
C0009378 (UMLS CUI [1])
C0037075 (UMLS CUI [2])
C0203075 (UMLS CUI [3])

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