ID

12844

Descripción

Radical Radiotherapy by External Beam Radiation Versus Radical Radiotherapy With Temporary Iridium Implant Plus External Beam Radiation in Carcinoma of the Prostate; ODM derived from: https://clinicaltrials.gov/show/NCT00548600

Link

https://clinicaltrials.gov/show/NCT00548600

Palabras clave

Versiones (1)
  1. 29/12/15 29/12/15 -
Subido en

29 de diciembre de 2015

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Prostate Cancer NCT00548600

Inglés

Eligibility Prostate Cancer NCT00548600

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
all patients must have histologically proven adenocarcinoma of the prostate
Descripción

all patients must have histologically proven adenocarcinoma of the prostate

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0600139
the primary tumour should be staged clinically b2 or c as classified by a.j.c. staging system
Descripción

the primary tumour should be staged clinically b2 or c as classified by a.j.c. staging system

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0027646
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients requiring transurethral prostatectomy (turp) prior to diagnosis
Descripción

patients requiring transurethral prostatectomy (turp) prior to diagnosis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0040771
presence of metastases identified by bone scan, chest x-ray or ct scan of the abdomen and pelvis, or staging lymphadenectomy
Descripción

presence of metastases identified by bone scan, chest x-ray or ct scan of the abdomen and pelvis, or staging lymphadenectomy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0027627
karnofsky performance status less than 80
Descripción

karnofsky performance status less than 80

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1520224
inadequate laboratory results: i.e. hb < 12 gm/litre, wbc < 3.5 x 10 per litre, platelets < 100 x 10/litre, urea > 13 mmol/litre, creatinine > 220 mmol/litre
Descripción

inadequate laboratory results: i.e. hb < 12 gm/litre, wbc < 3.5 x 10 per litre, platelets < 100 x 10/litre, urea > 13 mmol/litre, creatinine > 220 mmol/litre

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0019046
UMLS CUI [2]
C0023508
UMLS CUI [3]
C0005821
UMLS CUI [4]
C0041942
UMLS CUI [5]
C0201976
unfit for surgery for other medical reasons
Descripción

unfit for surgery for other medical reasons

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0852649
age above 75 years
Descripción

age above 75 years

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
failure to provide written informed consent
Descripción

failure to provide written informed consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
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Similar models

Eligibility Prostate Cancer NCT00548600

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
prostate carcinoma
Item
all patients must have histologically proven adenocarcinoma of the prostate
boolean
C0600139 (UMLS CUI [1])
tumor staging
Item
the primary tumour should be staged clinically b2 or c as classified by a.j.c. staging system
boolean
C0027646 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
transurethral prostatectomy
Item
patients requiring transurethral prostatectomy (turp) prior to diagnosis
boolean
C0040771 (UMLS CUI [1])
metastases
Item
presence of metastases identified by bone scan, chest x-ray or ct scan of the abdomen and pelvis, or staging lymphadenectomy
boolean
C0027627 (UMLS CUI [1])
performance status
Item
karnofsky performance status less than 80
boolean
C1520224 (UMLS CUI [1])
laboratory results
Item
inadequate laboratory results: i.e. hb < 12 gm/litre, wbc < 3.5 x 10 per litre, platelets < 100 x 10/litre, urea > 13 mmol/litre, creatinine > 220 mmol/litre
boolean
C0019046 (UMLS CUI [1])
C0023508 (UMLS CUI [2])
C0005821 (UMLS CUI [3])
C0041942 (UMLS CUI [4])
C0201976 (UMLS CUI [5])
contraindication to surgery
Item
unfit for surgery for other medical reasons
boolean
C0852649 (UMLS CUI [1])
age
Item
age above 75 years
boolean
C0001779 (UMLS CUI [1])
informed consent
Item
failure to provide written informed consent
boolean
C0021430 (UMLS CUI [1])
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