ID

21522

Descripción

Effect of Celecoxib on Survival in Patients With Advanced Non-Small Cell Lung Cancer Receiving Chemotherapy; ODM derived from: https://clinicaltrials.gov/show/NCT00300729

Link

https://clinicaltrials.gov/show/NCT00300729

Palabras clave

Versiones (1)
  1. 25-04-17 25-04-17 -
Subido en

25 april 2017

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Non-Small Cell Lung Cancer NCT00300729

Inglés

Eligibility Non-Small Cell Lung Cancer NCT00300729

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically or cytologically confirmed non-small cell lung cancer (nsclc).
Descripción

Non-small cell lung cancer

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0007131
age at least 18 years. no upper age limit.
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
disease stage iiib or iv.
Descripción

Tumor Stage

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1300072
performance status (who) 0-2
Descripción

Performance Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1518965
treatment with curative intent is not possible
Descripción

Curative Intention

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1276305
no prior chemotherapy for the present disease
Descripción

Prior chemotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1514457
planned treatment is palliative chemotherapy
Descripción

Palliative Chemotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C4272534
wbc count at least 3.0, platelet count at least 100
Descripción

WBC, Platelets

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023508
UMLS CUI [2]
C0005821
bilirubin < 1.5 * upper reference limit (url), asat and alat < 3 * url (<5 in case of liver metastases)
Descripción

Bilirubin, ASAT, ALAT

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1278039
UMLS CUI [2]
C0201899
UMLS CUI [3]
C0201836
calculated creatinine clearance at least 40 mg/ml
Descripción

Creatinine Clearance

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0373595
informed oral and written consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
regular use of nsaid (except asa at a dose of 50-100 mg daily)
Descripción

NSAID Use

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0003211
UMLS CUI [1,2]
C1524063
active duodenal ulcer, ongoing gastrointestinal bleeding or inflammatory bowel disease
Descripción

Duodenal ulcer, gastrointestinal bleeding or inflammatory bowel disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0013295
UMLS CUI [2]
C0017181
UMLS CUI [3]
C0021390
serious heart failure or serious liver disease
Descripción

Heart failure or Liver disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0018801
UMLS CUI [2]
C0023895
hypersensitivity to sulfonamides
Descripción

Hypersensitivity to sulfonamides

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0038760
pregnancy
Descripción

Pregnancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
lactation
Descripción

Lactation

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006147
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Similar models

Eligibility Non-Small Cell Lung Cancer NCT00300729

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Non-small cell lung cancer
Item
histologically or cytologically confirmed non-small cell lung cancer (nsclc).
boolean
C0007131 (UMLS CUI [1])
Age
Item
age at least 18 years. no upper age limit.
boolean
C0001779 (UMLS CUI [1])
Tumor Stage
Item
disease stage iiib or iv.
boolean
C1300072 (UMLS CUI [1])
Performance Status
Item
performance status (who) 0-2
boolean
C1518965 (UMLS CUI [1])
Curative Intention
Item
treatment with curative intent is not possible
boolean
C1276305 (UMLS CUI [1])
Prior chemotherapy
Item
no prior chemotherapy for the present disease
boolean
C1514457 (UMLS CUI [1])
Palliative Chemotherapy
Item
planned treatment is palliative chemotherapy
boolean
C4272534 (UMLS CUI [1])
WBC, Platelets
Item
wbc count at least 3.0, platelet count at least 100
boolean
C0023508 (UMLS CUI [1])
C0005821 (UMLS CUI [2])
Bilirubin, ASAT, ALAT
Item
bilirubin < 1.5 * upper reference limit (url), asat and alat < 3 * url (<5 in case of liver metastases)
boolean
C1278039 (UMLS CUI [1])
C0201899 (UMLS CUI [2])
C0201836 (UMLS CUI [3])
Creatinine Clearance
Item
calculated creatinine clearance at least 40 mg/ml
boolean
C0373595 (UMLS CUI [1])
Informed Consent
Item
informed oral and written consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
NSAID Use
Item
regular use of nsaid (except asa at a dose of 50-100 mg daily)
boolean
C0003211 (UMLS CUI [1,1])
C1524063 (UMLS CUI [1,2])
Duodenal ulcer, gastrointestinal bleeding or inflammatory bowel disease
Item
active duodenal ulcer, ongoing gastrointestinal bleeding or inflammatory bowel disease
boolean
C0013295 (UMLS CUI [1])
C0017181 (UMLS CUI [2])
C0021390 (UMLS CUI [3])
Heart failure or Liver disease
Item
serious heart failure or serious liver disease
boolean
C0018801 (UMLS CUI [1])
C0023895 (UMLS CUI [2])
Hypersensitivity to sulfonamides
Item
hypersensitivity to sulfonamides
boolean
C0020517 (UMLS CUI [1,1])
C0038760 (UMLS CUI [1,2])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Lactation
Item
lactation
boolean
C0006147 (UMLS CUI [1])
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