ID

14618

Beschreibung

Weekly Paclitaxel, Low-Dose Estramustine, and Carboplatin in the Treatment of Hormone Refractory Prostate Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT00193193

Link

https://clinicaltrials.gov/show/NCT00193193

Stichworte

  1. 24.04.16 24.04.16 -
Hochgeladen am

24. April 2016

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Prostate Cancer NCT00193193

Eligibility Prostate Cancer NCT00193193

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
adenocarcinoma of the prostate not curable with local treatment
Beschreibung

Prostate cancer

Datentyp

boolean

Alias
UMLS CUI [1]
C0600139
disease progression while receiving hormonal therapy
Beschreibung

Disease progression while hormonal therapy

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0242656
UMLS CUI [1,2]
C0279025
measurable or evaluable disease
Beschreibung

Measurable or evaluable disease

Datentyp

boolean

Alias
UMLS CUI [1]
C1513041
UMLS CUI [2]
C1516986
previous treatment with a maximum of one prior chemotherapy regimen
Beschreibung

Chemotherapy

Datentyp

boolean

Alias
UMLS CUI [1]
C0392920
ecog performance status 0, 1, or 2.
Beschreibung

ECOG performance status

Datentyp

boolean

Alias
UMLS CUI [1]
C1520224
adequate bone marrow, liver and kidney function
Beschreibung

Bone marrow, liver and kidney function

Datentyp

boolean

Alias
UMLS CUI [1]
C0232741
UMLS CUI [2]
C0005953
UMLS CUI [3]
C0232804
able to comprehend the nature of this study and give written informed consent
Beschreibung

Informed consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
you cannot participate in this study if any of the following apply to you:
Beschreibung

Exclusion criteria

Datentyp

boolean

Alias
UMLS CUI [1]
C0680251
age < 18 years
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
history of treatment for an invasive malignancy within five years
Beschreibung

Cancer treatment

Datentyp

boolean

Alias
UMLS CUI [1]
C0920425
significant heart disease
Beschreibung

Heart disease

Datentyp

boolean

Alias
UMLS CUI [1]
C0018799
please note: there are additional inclusion/exclusion criteria. the study center will determine if you meet all of the criteria. if you do not qualify for the trial, study personnel will explain the reasons. if you do qualify, study personnel will explain the trial in detail and answer any questions you may have.
Beschreibung

Inclusion and exclusion criteria

Datentyp

boolean

Alias
UMLS CUI [1]
C1512693
UMLS CUI [2]
C0680251

Ähnliche Modelle

Eligibility Prostate Cancer NCT00193193

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Prostate cancer
Item
adenocarcinoma of the prostate not curable with local treatment
boolean
C0600139 (UMLS CUI [1])
Disease progression while hormonal therapy
Item
disease progression while receiving hormonal therapy
boolean
C0242656 (UMLS CUI [1,1])
C0279025 (UMLS CUI [1,2])
Measurable or evaluable disease
Item
measurable or evaluable disease
boolean
C1513041 (UMLS CUI [1])
C1516986 (UMLS CUI [2])
Chemotherapy
Item
previous treatment with a maximum of one prior chemotherapy regimen
boolean
C0392920 (UMLS CUI [1])
ECOG performance status
Item
ecog performance status 0, 1, or 2.
boolean
C1520224 (UMLS CUI [1])
Bone marrow, liver and kidney function
Item
adequate bone marrow, liver and kidney function
boolean
C0232741 (UMLS CUI [1])
C0005953 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
Informed consent
Item
able to comprehend the nature of this study and give written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Exclusion criteria
Item
you cannot participate in this study if any of the following apply to you:
boolean
C0680251 (UMLS CUI [1])
Age
Item
age < 18 years
boolean
C0001779 (UMLS CUI [1])
Cancer treatment
Item
history of treatment for an invasive malignancy within five years
boolean
C0920425 (UMLS CUI [1])
Heart disease
Item
significant heart disease
boolean
C0018799 (UMLS CUI [1])
Inclusion and exclusion criteria
Item
please note: there are additional inclusion/exclusion criteria. the study center will determine if you meet all of the criteria. if you do not qualify for the trial, study personnel will explain the reasons. if you do qualify, study personnel will explain the trial in detail and answer any questions you may have.
boolean
C1512693 (UMLS CUI [1])
C0680251 (UMLS CUI [2])

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