ID

18407

Description

A Randomized Phase 3 Trial of Pemetrexed and Cisplatin Versus Gemcitabine and Cisplatin in Patients With Locally Advanced or Metastatic Non Small Cell Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00087711

Lien

https://clinicaltrials.gov/show/NCT00087711

Mots-clés

Versions (1)
  1. 03/11/2016 03/11/2016 -
Téléchargé le

3 novembre 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Non Small Cell Lung Carcinoma NCT00087711

Anglais

Eligibility Non Small Cell Lung Carcinoma NCT00087711

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis of nsclc stage iiib not amenable to curative treatment or stage iv.
Description

Non-Small Cell Lung Carcinoma | TNM clinical staging | Non-Small Cell Lung Carcinoma Amenable curative treatment

Type de données

boolean

Alias
UMLS CUI [1]
C0007131
UMLS CUI [2]
C3258246
UMLS CUI [3,1]
C0007131
UMLS CUI [3,2]
C3900053
UMLS CUI [3,3]
C1273390
no prior chemotherapy for lung cancer.
Description

Prior Chemotherapy Malignant neoplasm of lung

Type de données

boolean

Alias
UMLS CUI [1,1]
C1514457
UMLS CUI [1,2]
C0242379
patients must have at least one uni-dimensionally measurable lesion.
Description

Measurable Lesion Linear Quantity

Type de données

boolean

Alias
UMLS CUI [1,1]
C1513041
UMLS CUI [1,2]
C0205132
UMLS CUI [1,3]
C1265611
prior radiation therapy to less than 25% of bone marrow, whole pelvis not allowed. radiation must be completed at least 4 weeks prior to study enrollment.
Description

prior radiation therapy Bone Marrow Percentage | Therapeutic radiology procedure Whole-Pelvis | Therapeutic radiology procedure Completed

Type de données

boolean

Alias
UMLS CUI [1,1]
C0279134
UMLS CUI [1,2]
C0005953
UMLS CUI [1,3]
C0439165
UMLS CUI [2,1]
C1522449
UMLS CUI [2,2]
C3827467
UMLS CUI [3,1]
C1522449
UMLS CUI [3,2]
C0205197
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
treatment with any drug within the last 30 days that has not received regulatory approval.
Description

Drugs, Non-Prescription

Type de données

boolean

Alias
UMLS CUI [1]
C0013231
serious cardiac condition.
Description

Heart condition Serious

Type de données

boolean

Alias
UMLS CUI [1,1]
C3842523
UMLS CUI [1,2]
C0205404
serious medical disorder in addition to nsclc that would make it difficult for the patient to complete the study.
Description

Disease Serious In addition to Non-Small Cell Lung Carcinoma | Compliance behavior Limited

Type de données

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0205404
UMLS CUI [1,3]
C0332287
UMLS CUI [1,4]
C0007131
UMLS CUI [2,1]
C1321605
UMLS CUI [2,2]
C0439801
inability or unwillingness to take folic acid or vitamin b12 supplementation.
Description

Folic Acid Intake Unwilling | Vitamin B12 supplement Intake Unwilling

Type de données

boolean

Alias
UMLS CUI [1,1]
C0016410
UMLS CUI [1,2]
C1512806
UMLS CUI [1,3]
C0558080
UMLS CUI [2,1]
C3661610
UMLS CUI [2,2]
C1512806
UMLS CUI [2,3]
C0558080
presence of fluid retention that cannot be controlled by drainage.
Description

Body fluid retention | Drainage Unsuccessful

Type de données

boolean

Alias
UMLS CUI [1]
C0268000
UMLS CUI [2,1]
C0013103
UMLS CUI [2,2]
C1272705
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Similar models

Eligibility Non Small Cell Lung Carcinoma NCT00087711

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Non-Small Cell Lung Carcinoma | TNM clinical staging | Non-Small Cell Lung Carcinoma Amenable curative treatment
Item
diagnosis of nsclc stage iiib not amenable to curative treatment or stage iv.
boolean
C0007131 (UMLS CUI [1])
C3258246 (UMLS CUI [2])
C0007131 (UMLS CUI [3,1])
C3900053 (UMLS CUI [3,2])
C1273390 (UMLS CUI [3,3])
Prior Chemotherapy Malignant neoplasm of lung
Item
no prior chemotherapy for lung cancer.
boolean
C1514457 (UMLS CUI [1,1])
C0242379 (UMLS CUI [1,2])
Measurable Lesion Linear Quantity
Item
patients must have at least one uni-dimensionally measurable lesion.
boolean
C1513041 (UMLS CUI [1,1])
C0205132 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
prior radiation therapy Bone Marrow Percentage | Therapeutic radiology procedure Whole-Pelvis | Therapeutic radiology procedure Completed
Item
prior radiation therapy to less than 25% of bone marrow, whole pelvis not allowed. radiation must be completed at least 4 weeks prior to study enrollment.
boolean
C0279134 (UMLS CUI [1,1])
C0005953 (UMLS CUI [1,2])
C0439165 (UMLS CUI [1,3])
C1522449 (UMLS CUI [2,1])
C3827467 (UMLS CUI [2,2])
C1522449 (UMLS CUI [3,1])
C0205197 (UMLS CUI [3,2])
Item Group
C0680251 (UMLS CUI)
Drugs, Non-Prescription
Item
treatment with any drug within the last 30 days that has not received regulatory approval.
boolean
C0013231 (UMLS CUI [1])
Heart condition Serious
Item
serious cardiac condition.
boolean
C3842523 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
Disease Serious In addition to Non-Small Cell Lung Carcinoma | Compliance behavior Limited
Item
serious medical disorder in addition to nsclc that would make it difficult for the patient to complete the study.
boolean
C0012634 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0332287 (UMLS CUI [1,3])
C0007131 (UMLS CUI [1,4])
C1321605 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
Folic Acid Intake Unwilling | Vitamin B12 supplement Intake Unwilling
Item
inability or unwillingness to take folic acid or vitamin b12 supplementation.
boolean
C0016410 (UMLS CUI [1,1])
C1512806 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,3])
C3661610 (UMLS CUI [2,1])
C1512806 (UMLS CUI [2,2])
C0558080 (UMLS CUI [2,3])
Body fluid retention | Drainage Unsuccessful
Item
presence of fluid retention that cannot be controlled by drainage.
boolean
C0268000 (UMLS CUI [1])
C0013103 (UMLS CUI [2,1])
C1272705 (UMLS CUI [2,2])
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