ID

23465

Descripción

Study of Enzastaurin Versus Placebo With Pemetrexed for Patients With Advanced or Metastatic Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00530621

Link

https://clinicaltrials.gov/show/NCT00530621

Palabras clave

  1. 6/7/17 6/7/17 -
Subido en

6 de julio de 2017

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Non-small Cell Lung Cancer NCT00530621

Eligibility Non-small Cell Lung Cancer NCT00530621

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
laboratory confirmed diagnosis of nsclc with locally advanced or metastatic disease which cannot be cured.
Descripción

ID.1

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0007131
UMLS CUI [1,2]
C0278987
patients must have disease which progressed after 1 prior systemic cytotoxic chemotherapy regimen for advanced disease.
Descripción

ID.2

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0278940
at least 1 measurable lesion.
Descripción

ID.3

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0221198
must have stopped all previous systemic therapies for cancer for at least 2 weeks prior to enrollment.
Descripción

ID.4

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0444930
must be able to follow study guidelines and be able to show up for appointments.
Descripción

ID.5

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1321605
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
treatment within the last 30 days with a drug that has not received regulatory approval for any indication at the time of study entry.
Descripción

ID.6

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0013230
previous treatment with enzastaurin or pemetrexed.
Descripción

ID.7

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1327830
UMLS CUI [1,2]
C0210657
concurrent administration of any other antitumor therapy.
Descripción

ID.8

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2986475
inability to swallow tablets
Descripción

ID.9

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0566357
UMLS CUI [1,2]
C0039225
pregnant or breastfeeding
Descripción

ID.10

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0006147

Similar models

Eligibility Non-small Cell Lung Cancer NCT00530621

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
laboratory confirmed diagnosis of nsclc with locally advanced or metastatic disease which cannot be cured.
boolean
C0007131 (UMLS CUI [1,1])
C0278987 (UMLS CUI [1,2])
ID.2
Item
patients must have disease which progressed after 1 prior systemic cytotoxic chemotherapy regimen for advanced disease.
boolean
C0278940 (UMLS CUI [1])
ID.3
Item
at least 1 measurable lesion.
boolean
C0221198 (UMLS CUI [1])
ID.4
Item
must have stopped all previous systemic therapies for cancer for at least 2 weeks prior to enrollment.
boolean
C0087111 (UMLS CUI [1,1])
C0444930 (UMLS CUI [1,2])
ID.5
Item
must be able to follow study guidelines and be able to show up for appointments.
boolean
C1321605 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
ID.6
Item
treatment within the last 30 days with a drug that has not received regulatory approval for any indication at the time of study entry.
boolean
C0013230 (UMLS CUI [1])
ID.7
Item
previous treatment with enzastaurin or pemetrexed.
boolean
C1327830 (UMLS CUI [1,1])
C0210657 (UMLS CUI [1,2])
ID.8
Item
concurrent administration of any other antitumor therapy.
boolean
C2986475 (UMLS CUI [1])
ID.9
Item
inability to swallow tablets
boolean
C0566357 (UMLS CUI [1,1])
C0039225 (UMLS CUI [1,2])
ID.10
Item
pregnant or breastfeeding
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])

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