Informazione: All download services should be available again. In case you still experience any issues, please contact us.
Informazione:
Errore:
ID
14618
Descrizione
Weekly Paclitaxel, Low-Dose Estramustine, and Carboplatin in the Treatment of Hormone Refractory Prostate Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT00193193
collegamento
https://clinicaltrials.gov/show/NCT00193193
Keywords
versioni (1)
- 24/04/16 24/04/16 -
Caricato su
24 aprile 2016
DOI
Per favore, per richiedere un accesso.
Licenza
Creative Commons BY 4.0
Commenti del modello :
Puoi commentare il modello dati qui. Tramite i fumetti nei gruppi di articoli e articoli è possibile aggiungere commenti a quelli in modo specifico.
Commenti del gruppo di articoli per :
Commenti dell'articolo per :
Per scaricare i modelli di dati devi essere registrato. Per favore accesso o registrati GRATIS.
Eligibility Prostate Cancer NCT00193193
Eligibility Prostate Cancer NCT00193193
- StudyEvent: Eligibility
Similar models
Eligibility Prostate Cancer NCT00193193
- StudyEvent: Eligibility
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
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])
C0279025 (UMLS CUI [1,2])
Measurable or evaluable disease
Item
measurable or evaluable disease
boolean
C1513041 (UMLS CUI [1])
C1516986 (UMLS CUI [2])
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])
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])
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])
C0680251 (UMLS CUI [2])