ID

36846

Description

Early Investigation of High Precision Radiotherapy Prior to Commencing Standard Radiotherapy for Prostate Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT02004223

Link

https://clinicaltrials.gov/show/NCT02004223

Keywords

  1. 6/15/19 6/15/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

June 15, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Prostate Cancer NCT02004223

Eligibility Prostate Cancer NCT02004223

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically proven prostate adenocarcinoma
Description

Adenocarcinoma of prostate

Data type

boolean

Alias
UMLS CUI [1]
C0007112
psa obtained within three months prior to enrollment.
Description

Prostate-Specific Antigen

Data type

boolean

Alias
UMLS CUI [1]
C0138741
international prostate symptom score (i-pss) score <15
Description

International Prostate Symptom Score

Data type

boolean

Alias
UMLS CUI [1]
C1998280
no contraindication to mri (pacemaker, severe claustrophobia)
Description

Medical contraindication Absent MRI | Artificial cardiac pacemaker | Claustrophobia Severe

Data type

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0332197
UMLS CUI [1,3]
C0024485
UMLS CUI [2]
C0030163
UMLS CUI [3,1]
C0008909
UMLS CUI [3,2]
C0205082
patient must be able to have fiducial markers placed in the prostate (if on anticoagulants, must be cleared by lmo or cardiologist).
Description

Fiducial marker placement Prostate | Anticoagulants

Data type

boolean

Alias
UMLS CUI [1,1]
C3888577
UMLS CUI [1,2]
C0033572
UMLS CUI [2]
C0003280
ecog performance status 0-2
Description

ECOG performance status

Data type

boolean

Alias
UMLS CUI [1]
C1520224
ability to understand and the willingness to sign a written informed consent document.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
previous pelvic radiotherapy
Description

Radiotherapy to pelvis

Data type

boolean

Alias
UMLS CUI [1]
C1536155
prior total prostatectomy
Description

Radical prostatectomy

Data type

boolean

Alias
UMLS CUI [1]
C0194810
unwilling or unable to give 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
unwilling or unable to complete quality of life questionnaires.
Description

Quality of life questionnaire Completion Unwilling | Quality of life questionnaire Completion Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C0451149
UMLS CUI [1,2]
C0205197
UMLS CUI [1,3]
C0558080
UMLS CUI [2,1]
C0451149
UMLS CUI [2,2]
C0205197
UMLS CUI [2,3]
C1299582

Similar models

Eligibility Prostate Cancer NCT02004223

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Adenocarcinoma of prostate
Item
histologically proven prostate adenocarcinoma
boolean
C0007112 (UMLS CUI [1])
Prostate-Specific Antigen
Item
psa obtained within three months prior to enrollment.
boolean
C0138741 (UMLS CUI [1])
International Prostate Symptom Score
Item
international prostate symptom score (i-pss) score <15
boolean
C1998280 (UMLS CUI [1])
Medical contraindication Absent MRI | Artificial cardiac pacemaker | Claustrophobia Severe
Item
no contraindication to mri (pacemaker, severe claustrophobia)
boolean
C1301624 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0024485 (UMLS CUI [1,3])
C0030163 (UMLS CUI [2])
C0008909 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
Fiducial marker placement Prostate | Anticoagulants
Item
patient must be able to have fiducial markers placed in the prostate (if on anticoagulants, must be cleared by lmo or cardiologist).
boolean
C3888577 (UMLS CUI [1,1])
C0033572 (UMLS CUI [1,2])
C0003280 (UMLS CUI [2])
ECOG performance status
Item
ecog performance status 0-2
boolean
C1520224 (UMLS CUI [1])
Informed Consent
Item
ability to understand and the willingness to sign a written informed consent document.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Radiotherapy to pelvis
Item
previous pelvic radiotherapy
boolean
C1536155 (UMLS CUI [1])
Radical prostatectomy
Item
prior total prostatectomy
boolean
C0194810 (UMLS CUI [1])
Informed Consent Unwilling | Informed Consent Unable
Item
unwilling or unable to give informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
Quality of life questionnaire Completion Unwilling | Quality of life questionnaire Completion Unable
Item
unwilling or unable to complete quality of life questionnaires.
boolean
C0451149 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,3])
C0451149 (UMLS CUI [2,1])
C0205197 (UMLS CUI [2,2])
C1299582 (UMLS CUI [2,3])

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