ID

13595

Descripción

Shorter Radiation Schedule for the Treatment of Prostate Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00201916

Link

https://clinicaltrials.gov/show/NCT00201916

Palabras clave

  1. 18/2/16 18/2/16 -
Subido en

18 de febrero de 2016

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Prostate Cancer NCT00201916

Eligibility Prostate Cancer NCT00201916

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologic diagnosis of adenocarcinoma of the prostate with no evidence of metastatic disease to the nodes, bone or lung
Descripción

prostate carcinoma, no metastases

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0600139
UMLS CUI [2]
C0027627
stage t1a moderately or poorly differentiated, t1b, t1c or t2 by the current uicc-tnm classification
Descripción

tumor stage

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1300072
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
psa > 40 mcg/l
Descripción

psa

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0138741
previous therapy for carcinoma of the prostate other than biopsy or turp, including patients previously on hormone therapy for treatment of their prostate cancer
Descripción

previous treatment

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0087111
UMLS CUI [2]
C0600139
prior or active malignancy other than non-melanoma skin cancer; or colon or thyroid cancer treated a minimum of five years prior to study entry and presumed cured
Descripción

malignancies

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006826
simulated volume exceeds 1000 cm3
Descripción

tumor volume

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0475276
previous pelvic radiotherapy
Descripción

previous pelvic radiotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0030797
inflammatory bowel disease
Descripción

inflammatory bowel disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021390
serious non-malignant disease which would preclude radiotherapy or surgical biopsy
Descripción

comorbidity precluding radiotherapy or surgical biopsy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
geographic inaccessibility for follow-up
Descripción

geographic inaccessibility for follow-up

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1321605
psychiatric or addictive disorder which would preclude obtaining informed consent or adherence to protocol
Descripción

psychiatric or addictive disorder precluding consent or compliance

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
unable to commence radiation therapy within 26 weeks of the date of last prostatic biopsy
Descripción

unable to commence radiation therapy within 26 weeks

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1321605
failure to give informed consent to participate in the study
Descripción

failure to give informed consent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0439801

Similar models

Eligibility Prostate Cancer NCT00201916

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
prostate carcinoma, no metastases
Item
histologic diagnosis of adenocarcinoma of the prostate with no evidence of metastatic disease to the nodes, bone or lung
boolean
C0600139 (UMLS CUI [1])
C0027627 (UMLS CUI [2])
tumor stage
Item
stage t1a moderately or poorly differentiated, t1b, t1c or t2 by the current uicc-tnm classification
boolean
C1300072 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
psa
Item
psa > 40 mcg/l
boolean
C0138741 (UMLS CUI [1])
previous treatment
Item
previous therapy for carcinoma of the prostate other than biopsy or turp, including patients previously on hormone therapy for treatment of their prostate cancer
boolean
C0087111 (UMLS CUI [1])
C0600139 (UMLS CUI [2])
malignancies
Item
prior or active malignancy other than non-melanoma skin cancer; or colon or thyroid cancer treated a minimum of five years prior to study entry and presumed cured
boolean
C0006826 (UMLS CUI [1])
tumor volume
Item
simulated volume exceeds 1000 cm3
boolean
C0475276 (UMLS CUI [1])
previous pelvic radiotherapy
Item
previous pelvic radiotherapy
boolean
C1522449 (UMLS CUI [1,1])
C0030797 (UMLS CUI [1,2])
inflammatory bowel disease
Item
inflammatory bowel disease
boolean
C0021390 (UMLS CUI [1])
comorbidity precluding radiotherapy or surgical biopsy
Item
serious non-malignant disease which would preclude radiotherapy or surgical biopsy
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
geographic inaccessibility for follow-up
Item
geographic inaccessibility for follow-up
boolean
C1321605 (UMLS CUI [1])
psychiatric or addictive disorder precluding consent or compliance
Item
psychiatric or addictive disorder which would preclude obtaining informed consent or adherence to protocol
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
unable to commence radiation therapy within 26 weeks
Item
unable to commence radiation therapy within 26 weeks of the date of last prostatic biopsy
boolean
C1321605 (UMLS CUI [1])
failure to give informed consent
Item
failure to give informed consent to participate in the study
boolean
C0021430 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])

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