ID

17570

Descripción

A Trial of Strontium +/- Cisplatin for the Palliation of Bone Pain Secondary to Hormone Refractory Prostate Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00156884

Link

https://clinicaltrials.gov/show/NCT00156884

Palabras clave

Versiones (1)
  1. 25/9/16 25/9/16 -
Subido en

25 de septiembre de 2016

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Hormone Refractory Prostate Cancer NCT00156884

Inglés

Eligibility Hormone Refractory Prostate Cancer NCT00156884

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
adenocarcinoma of the prostate
Descripción

Adenocarcinoma of prostate

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0007112
life expectancy > 3 months,
Descripción

Life Expectancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023671
symptomatic from bone metastases
Descripción

Secondary malignant neoplasm of bone Symptomatic

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0153690
UMLS CUI [1,2]
C0231220
radiologic evidence of metastatic bone disease
Descripción

Bone Disease Metastatic Evidence Radiologic

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0005940
UMLS CUI [1,2]
C0036525
UMLS CUI [1,3]
C3887511
UMLS CUI [1,4]
C0205483
stable level of pain control
Descripción

Pain control Stable status

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1304888
UMLS CUI [1,2]
C0205360
>18 years
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
ability to complete assessments
Descripción

Assessment Complete Ability

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1516048
UMLS CUI [1,2]
C0205197
UMLS CUI [1,3]
C0085732
prior treatment (chemo) > 4 weeks previous
Descripción

Prior Chemotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1514457
discontinued anti-androgens for > 4 weeks
Descripción

Androgen Antagonists Discontinued

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0002842
UMLS CUI [1,2]
C1444662
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
prior strontium therapy
Descripción

Strontium

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0038467
previous hemibody rt within 6 weeks
Descripción

Therapeutic radiology procedure Hemibody

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C3846139
previous cytotoxic chemotherapy within 4 weeks
Descripción

Cytotoxic Chemotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0677881
use of bisphosphonate medications within 4 weeks
Descripción

Diphosphonates

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0012544
change in steroid dose within 4 weeks
Descripción

Steroid Dose Change

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0038317
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0392747
active uncontrolled infection
Descripción

Communicable Disease Uncontrolled

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0009450
UMLS CUI [1,2]
C0205318
impending or present spinal cord compression
Descripción

Compression of spinal cord Impending | Compression of spinal cord

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0037926
UMLS CUI [1,2]
C0332190
UMLS CUI [2]
C0037926
significant neurological disorder
Descripción

nervous system disorder Significant

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0027765
UMLS CUI [1,2]
C0750502
impending pathological fracture
Descripción

Pathological fracture Impending

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0016663
UMLS CUI [1,2]
C0332190
severe urinary incontinence
Descripción

Urinary Incontinence Severe

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0042024
UMLS CUI [1,2]
C0205082
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Similar models

Eligibility Hormone Refractory Prostate Cancer NCT00156884

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Adenocarcinoma of prostate
Item
adenocarcinoma of the prostate
boolean
C0007112 (UMLS CUI [1])
Life Expectancy
Item
life expectancy > 3 months,
boolean
C0023671 (UMLS CUI [1])
Secondary malignant neoplasm of bone Symptomatic
Item
symptomatic from bone metastases
boolean
C0153690 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
Bone Disease Metastatic Evidence Radiologic
Item
radiologic evidence of metastatic bone disease
boolean
C0005940 (UMLS CUI [1,1])
C0036525 (UMLS CUI [1,2])
C3887511 (UMLS CUI [1,3])
C0205483 (UMLS CUI [1,4])
Pain control Stable status
Item
stable level of pain control
boolean
C1304888 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
Age
Item
>18 years
boolean
C0001779 (UMLS CUI [1])
Assessment Complete Ability
Item
ability to complete assessments
boolean
C1516048 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,3])
Prior Chemotherapy
Item
prior treatment (chemo) > 4 weeks previous
boolean
C1514457 (UMLS CUI [1])
Androgen Antagonists Discontinued
Item
discontinued anti-androgens for > 4 weeks
boolean
C0002842 (UMLS CUI [1,1])
C1444662 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Strontium
Item
prior strontium therapy
boolean
C0038467 (UMLS CUI [1])
Therapeutic radiology procedure Hemibody
Item
previous hemibody rt within 6 weeks
boolean
C1522449 (UMLS CUI [1,1])
C3846139 (UMLS CUI [1,2])
Cytotoxic Chemotherapy
Item
previous cytotoxic chemotherapy within 4 weeks
boolean
C0677881 (UMLS CUI [1])
Diphosphonates
Item
use of bisphosphonate medications within 4 weeks
boolean
C0012544 (UMLS CUI [1])
Steroid Dose Change
Item
change in steroid dose within 4 weeks
boolean
C0038317 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0392747 (UMLS CUI [1,3])
Communicable Disease Uncontrolled
Item
active uncontrolled infection
boolean
C0009450 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
Compression of spinal cord Impending | Compression of spinal cord
Item
impending or present spinal cord compression
boolean
C0037926 (UMLS CUI [1,1])
C0332190 (UMLS CUI [1,2])
C0037926 (UMLS CUI [2])
nervous system disorder Significant
Item
significant neurological disorder
boolean
C0027765 (UMLS CUI [1,1])
C0750502 (UMLS CUI [1,2])
Pathological fracture Impending
Item
impending pathological fracture
boolean
C0016663 (UMLS CUI [1,1])
C0332190 (UMLS CUI [1,2])
Urinary Incontinence Severe
Item
severe urinary incontinence
boolean
C0042024 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
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