Eligibility Prostate Cancer NCT00663832

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
hrpc patients
Beschreibung

Hormone refractory prostate cancer

Datentyp

boolean

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

Disease Progression

Datentyp

boolean

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

Self care | Ability Performance Light Work

Datentyp

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
Beschreibung

Contraceptive methods Willing

Datentyp

boolean

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

Exclusion Criteria

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

Cancer Other Disease length | Curative treatment Absent

Datentyp

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
Beschreibung

Prior radiation therapy

Datentyp

boolean

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

Radiopharmaceuticals | Strontium | Samarium

Datentyp

boolean

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

Decreased cardiac function

Datentyp

boolean

Alias
UMLS CUI [1]
C0232166
heart disease
Beschreibung

Heart Disease

Datentyp

boolean

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

Liver disease | Kidney Disease | Liver Dysfunction | Renal Insufficiency

Datentyp

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
Beschreibung

Eligibility Criteria Study Protocol

Datentyp

boolean

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

Ähnliche Modelle

Eligibility Prostate Cancer NCT00663832

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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])