ID

17233

Beskrivning

Radiation Therapy in Treating Patients With Stage I, Stage II, or Stage III Prostate Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00258466

Länk

https://clinicaltrials.gov/show/NCT00258466

Nyckelord

  1. 2016-09-01 2016-09-01 -
Uppladdad den

1 september 2016

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Prostate Cancer NCT00258466

Eligibility Prostate Cancer NCT00258466

Criteria
Beskrivning

Criteria

histologically confirmed adenocarcinoma of the prostate
Beskrivning

Adenocarcinoma of the prostate

Datatyp

boolean

Alias
UMLS CUI [1]
C0007112
stage i-iii disease (t1-t3, n0, m0)
Beskrivning

Tumor stage

Datatyp

boolean

Alias
UMLS CUI [1]
C1300072
no clinical or radiographic evidence of metastasis
Beskrivning

Metastasis

Datatyp

boolean

Alias
UMLS CUI [1]
C0027627
if prostate-specific antigen (psa) ≥ 10.0 ng/ml and gleason score is 7, a radioisotope bone scan must show no evidence of metastasis
Beskrivning

Radioisotope bone scan must show no evidence of metastasis

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0203668
UMLS CUI [1,2]
C0027627
no evidence of lymphatic or visceral metastases of the abdomen or pelvis on ct scan or mri
Beskrivning

no evidence of lymphatic or visceral metastases

Datatyp

boolean

Alias
UMLS CUI [1]
C0024232
UMLS CUI [2,1]
C0027627
UMLS CUI [2,2]
C0442045
psa ≤ 20 ng/ml
Beskrivning

PSA

Datatyp

boolean

Alias
UMLS CUI [1]
C0201544
gleason score ≤ 7 (if stage t3 , score must be < 7)
Beskrivning

gleason score

Datatyp

boolean

Alias
UMLS CUI [1]
C0332326
patient characteristics:
Beskrivning

patient characteristics

Datatyp

boolean

Alias
UMLS CUI [1]
C0815172
performance status: not specified
Beskrivning

performance status

Datatyp

boolean

Alias
UMLS CUI [1]
C1518965
life expectancy: more than 10 years
Beskrivning

life expectancy

Datatyp

boolean

Alias
UMLS CUI [1]
C0023671
hematopoietic: not specified
Beskrivning

hematopoiesis

Datatyp

boolean

Alias
UMLS CUI [1]
C0018951
hepatic: not specified
Beskrivning

Hepatic function

Datatyp

boolean

Alias
UMLS CUI [1]
C0232741
renal: not specified
Beskrivning

Renal function

Datatyp

boolean

Alias
UMLS CUI [1]
C0232804
other: no other malignancy within the past 5 years except basal cell or squamous cell skin cancer
Beskrivning

Malignancy

Datatyp

boolean

Alias
UMLS CUI [1]
C0006826
prior concurrent therapy:
Beskrivning

concurrent therapy

Datatyp

boolean

Alias
UMLS CUI [1]
C0009429
endocrine therapy
Beskrivning

endocrine therapy

Datatyp

boolean

Alias
UMLS CUI [1]
C0279025
prior hormonal therapy allowed provided it was initiated no more than 2 months ago, and may include the following:
Beskrivning

Hormonal therapy

Datatyp

boolean

Alias
UMLS CUI [1]
C0279025
luteinizing hormone-releasing hormone agonists (e.g., goserelin, leuprolide)
Beskrivning

luteinizing hormone-releasing hormone agonists

Datatyp

boolean

Alias
UMLS CUI [1]
C1518041
anti-androgens (e.g., flutamide, bicalutamide)
Beskrivning

anti-androgens

Datatyp

boolean

Alias
UMLS CUI [1]
C0002842
radiotherapy
Beskrivning

Radiotherapy

Datatyp

boolean

Alias
UMLS CUI [1]
C1522449
no prior pelvic irradiation
Beskrivning

pelvic irradiation

Datatyp

boolean

Alias
UMLS CUI [1]
C0747411
surgery
Beskrivning

Surgery

Datatyp

boolean

Alias
UMLS CUI [1]
C0543467
no prior radical prostatectomy
Beskrivning

radical prostatectomy

Datatyp

boolean

Alias
UMLS CUI [1]
C0194810

Similar models

Eligibility Prostate Cancer NCT00258466

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Adenocarcinoma of the prostate
Item
histologically confirmed adenocarcinoma of the prostate
boolean
C0007112 (UMLS CUI [1])
Tumor stage
Item
stage i-iii disease (t1-t3, n0, m0)
boolean
C1300072 (UMLS CUI [1])
Metastasis
Item
no clinical or radiographic evidence of metastasis
boolean
C0027627 (UMLS CUI [1])
Radioisotope bone scan must show no evidence of metastasis
Item
if prostate-specific antigen (psa) ≥ 10.0 ng/ml and gleason score is 7, a radioisotope bone scan must show no evidence of metastasis
boolean
C0203668 (UMLS CUI [1,1])
C0027627 (UMLS CUI [1,2])
no evidence of lymphatic or visceral metastases
Item
no evidence of lymphatic or visceral metastases of the abdomen or pelvis on ct scan or mri
boolean
C0024232 (UMLS CUI [1])
C0027627 (UMLS CUI [2,1])
C0442045 (UMLS CUI [2,2])
PSA
Item
psa ≤ 20 ng/ml
boolean
C0201544 (UMLS CUI [1])
gleason score
Item
gleason score ≤ 7 (if stage t3 , score must be < 7)
boolean
C0332326 (UMLS CUI [1])
patient characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
performance status
Item
performance status: not specified
boolean
C1518965 (UMLS CUI [1])
life expectancy
Item
life expectancy: more than 10 years
boolean
C0023671 (UMLS CUI [1])
hematopoiesis
Item
hematopoietic: not specified
boolean
C0018951 (UMLS CUI [1])
Hepatic function
Item
hepatic: not specified
boolean
C0232741 (UMLS CUI [1])
Renal function
Item
renal: not specified
boolean
C0232804 (UMLS CUI [1])
Malignancy
Item
other: no other malignancy within the past 5 years except basal cell or squamous cell skin cancer
boolean
C0006826 (UMLS CUI [1])
concurrent therapy
Item
prior concurrent therapy:
boolean
C0009429 (UMLS CUI [1])
endocrine therapy
Item
endocrine therapy
boolean
C0279025 (UMLS CUI [1])
Hormonal therapy
Item
prior hormonal therapy allowed provided it was initiated no more than 2 months ago, and may include the following:
boolean
C0279025 (UMLS CUI [1])
luteinizing hormone-releasing hormone agonists
Item
luteinizing hormone-releasing hormone agonists (e.g., goserelin, leuprolide)
boolean
C1518041 (UMLS CUI [1])
anti-androgens
Item
anti-androgens (e.g., flutamide, bicalutamide)
boolean
C0002842 (UMLS CUI [1])
Radiotherapy
Item
radiotherapy
boolean
C1522449 (UMLS CUI [1])
pelvic irradiation
Item
no prior pelvic irradiation
boolean
C0747411 (UMLS CUI [1])
Surgery
Item
surgery
boolean
C0543467 (UMLS CUI [1])
radical prostatectomy
Item
no prior radical prostatectomy
boolean
C0194810 (UMLS CUI [1])

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