ID

31570

Descripción

A Dose Finding Study With I.V. Panobinostat (LBH589), Docetaxel, and Prednisone in Patients With Hormone Refractory Prostate Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00663832

Link

https://clinicaltrials.gov/show/NCT00663832

Palabras clave

Versiones (1)
  1. 5/9/18 5/9/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

5 de septiembre de 2018

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Prostate Cancer NCT00663832

Inglés

Eligibility Prostate Cancer NCT00663832

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
hrpc patients
Descripción

Hormone refractory prostate cancer

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1328504
evidence of disease progression
Descripción

Disease Progression

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0242656
self care, able to perform light work activities
Descripción

Self care | Ability Performance Light Work

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3872897
UMLS CUI [2,1]
C0085732
UMLS CUI [2,2]
C0597198
UMLS CUI [2,3]
C2987220
willing to use contraception throughout the study and for 12 weeks after study completion
Descripción

Contraceptive methods Willing

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0700589
UMLS CUI [1,2]
C0600109
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of other cancers not curatively treated with no evidence of disease for more than 5 years.
Descripción

Cancer Other Disease length | Curative treatment Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1707251
UMLS CUI [1,2]
C0872146
UMLS CUI [2,1]
C1273390
UMLS CUI [2,2]
C0332197
prior radiotherapy within 3 weeks of starting study treatment
Descripción

Prior radiation therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0279134
prior radiopharmaceuticals (strontium, samarium).
Descripción

Radiopharmaceuticals | Strontium | Samarium

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0182638
UMLS CUI [2]
C0038467
UMLS CUI [3]
C0036147
impaired cardiac function
Descripción

Decreased cardiac function

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0232166
heart disease
Descripción

Heart Disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0018799
liver or renal disease with impaired functions.
Descripción

Liver disease | Kidney Disease | Liver Dysfunction | Renal Insufficiency

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023895
UMLS CUI [2]
C0022658
UMLS CUI [3]
C0086565
UMLS CUI [4]
C1565489
other protocol-defined inclusion/exclusion criteria may apply
Descripción

Eligibility Criteria Study Protocol

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1516637
UMLS CUI [1,2]
C2348563
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Similar models

Eligibility Prostate Cancer NCT00663832

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Hormone refractory prostate cancer
Item
hrpc patients
boolean
C1328504 (UMLS CUI [1])
Disease Progression
Item
evidence of disease progression
boolean
C0242656 (UMLS CUI [1])
Self care | Ability Performance Light Work
Item
self care, able to perform light work activities
boolean
C3872897 (UMLS CUI [1])
C0085732 (UMLS CUI [2,1])
C0597198 (UMLS CUI [2,2])
C2987220 (UMLS CUI [2,3])
Contraceptive methods Willing
Item
willing to use contraception throughout the study and for 12 weeks after study completion
boolean
C0700589 (UMLS CUI [1,1])
C0600109 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Cancer Other Disease length | Curative treatment Absent
Item
history of other cancers not curatively treated with no evidence of disease for more than 5 years.
boolean
C1707251 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
C1273390 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Prior radiation therapy
Item
prior radiotherapy within 3 weeks of starting study treatment
boolean
C0279134 (UMLS CUI [1])
Radiopharmaceuticals | Strontium | Samarium
Item
prior radiopharmaceuticals (strontium, samarium).
boolean
C0182638 (UMLS CUI [1])
C0038467 (UMLS CUI [2])
C0036147 (UMLS CUI [3])
Decreased cardiac function
Item
impaired cardiac function
boolean
C0232166 (UMLS CUI [1])
Heart Disease
Item
heart disease
boolean
C0018799 (UMLS CUI [1])
Liver disease | Kidney Disease | Liver Dysfunction | Renal Insufficiency
Item
liver or renal disease with impaired functions.
boolean
C0023895 (UMLS CUI [1])
C0022658 (UMLS CUI [2])
C0086565 (UMLS CUI [3])
C1565489 (UMLS CUI [4])
Eligibility Criteria Study Protocol
Item
other protocol-defined inclusion/exclusion criteria may apply
boolean
C1516637 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
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