ID

13876

Description

Prostate Accurately Targeted Radiotherapy Investigation of Overall Treatment Time; ODM derived from: https://clinicaltrials.gov/show/NCT01423474

Link

https://clinicaltrials.gov/show/NCT01423474

Keywords

Versions (1)
  1. 3/13/16 3/13/16 -
Uploaded on

March 13, 2016

DOI

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License

Creative Commons BY 4.0
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Eligibility Prostatic Neoplasms NCT01423474

English

Eligibility Prostatic Neoplasms NCT01423474

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
low or intermediate risk prostate cancer patients as defined by:
Description

prostate cancer

Data type

boolean

Alias
UMLS CUI [1]
C0600139
clinical stage t1-2b, gleason score <=7, and psa <=20 ng/ml
Description

tumor stage; gleason score; prostate specific antigen

Data type

boolean

Alias
UMLS CUI [1]
C1300072
UMLS CUI [2]
C3203027
UMLS CUI [3]
C0138741
age >= 18 years
Description

age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
androgen deprivation therapy (lhrh-agonists or antiandrogens) >6 months
Description

Antiandrogen therapy

Data type

boolean

Alias
UMLS CUI [1]
C0279492
prior pelvic radiotherapy
Description

pelvic radiotherapy

Data type

boolean

Alias
UMLS CUI [1]
C0436276
anticoagulation medication (if unsafe to discontinue for gold seed insertion)
Description

anticoagulation medication

Data type

boolean

Alias
UMLS CUI [1]
C0003280
diagnosis of bleeding diathesis
Description

bleeding diathesis

Data type

boolean

Alias
UMLS CUI [1]
C0005779
large prostate (>90cm3) on imaging
Description

large prostate

Data type

boolean

Alias
UMLS CUI [1]
C0426732
immunosuppressive medications
Description

immunosuppressive medications

Data type

boolean

Alias
UMLS CUI [1]
C0021081
inflammatory bowel disease
Description

inflammatory bowel disease

Data type

boolean

Alias
UMLS CUI [1]
C0021390
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Similar models

Eligibility Prostatic Neoplasms NCT01423474

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
prostate cancer
Item
low or intermediate risk prostate cancer patients as defined by:
boolean
C0600139 (UMLS CUI [1])
tumor stage; gleason score; prostate specific antigen
Item
clinical stage t1-2b, gleason score <=7, and psa <=20 ng/ml
boolean
C1300072 (UMLS CUI [1])
C3203027 (UMLS CUI [2])
C0138741 (UMLS CUI [3])
age
Item
age >= 18 years
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Antiandrogen therapy
Item
androgen deprivation therapy (lhrh-agonists or antiandrogens) >6 months
boolean
C0279492 (UMLS CUI [1])
pelvic radiotherapy
Item
prior pelvic radiotherapy
boolean
C0436276 (UMLS CUI [1])
anticoagulation medication
Item
anticoagulation medication (if unsafe to discontinue for gold seed insertion)
boolean
C0003280 (UMLS CUI [1])
bleeding diathesis
Item
diagnosis of bleeding diathesis
boolean
C0005779 (UMLS CUI [1])
large prostate
Item
large prostate (>90cm3) on imaging
boolean
C0426732 (UMLS CUI [1])
immunosuppressive medications
Item
immunosuppressive medications
boolean
C0021081 (UMLS CUI [1])
inflammatory bowel disease
Item
inflammatory bowel disease
boolean
C0021390 (UMLS CUI [1])
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