ID

18478

Beschreibung

A Trial of Carboplatin and Gemcitabine Versus Gemcitabine Alone in Patients With Non-Small-Cell Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00190710

Link

https://clinicaltrials.gov/show/NCT00190710

Stichworte

Versionen (1)
  1. 07.11.16 07.11.16 -
Hochgeladen am

7. November 2016

DOI

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Lizenz

Creative Commons BY 4.0
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Eligibility Non-Small Cell Lung Cancer NCT00190710

Englisch

Eligibility Non-Small Cell Lung Cancer NCT00190710

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologic or cytologic new diagnosis of nsclc, stage iiib with a cytologically positive pleural or pericardial effusion or stage iv.
Beschreibung

Non-Small Cell Lung Carcinoma | TNM clinical staging | Pleural effusion disorder | Pericardial effusion

Datentyp

boolean

Alias
UMLS CUI [1]
C0007131
UMLS CUI [2]
C3258246
UMLS CUI [3]
C0032227
UMLS CUI [4]
C0031039
no prior chemotherapy, including adjuvant or neoadjuvant therapy, for the treatment of nsclc.
Beschreibung

Prior Chemotherapy Non-Small Cell Lung Carcinoma | Adjuvant therapy Non-Small Cell Lung Carcinoma | Neoadjuvant Therapy Non-Small Cell Lung Carcinoma

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1514457
UMLS CUI [1,2]
C0007131
UMLS CUI [2,1]
C0677850
UMLS CUI [2,2]
C0007131
UMLS CUI [3,1]
C0600558
UMLS CUI [3,2]
C0007131
ecog performance status of 2 .
Beschreibung

ECOG performance status

Datentyp

boolean

Alias
UMLS CUI [1]
C1520224
patients must be at least 3 weeks since major surgery. patients must be at least 1 week since surgery, such as mediastinoscopy, pleuroscopy, or thoracostomy.
Beschreibung

major surgery | Operative Surgical Procedures | Mediastinoscopy | Thoracoscopy | Thoracostomy

Datentyp

boolean

Alias
UMLS CUI [1]
C0679637
UMLS CUI [2]
C0543467
UMLS CUI [3]
C0025065
UMLS CUI [4]
C0039989
UMLS CUI [5]
C0039990
patients must have measurable disease, defined as lesions that can be accurately measured in at least 1 dimension (longest diameter to be recorded) as greater than or equal to 20 mm with conventional techniques or as greater than 10 mm with spiral ct scan.
Beschreibung

Measurable Disease Dimensions Quantity | Lesion Longest Diameter | Measurement technique conventional | Tomography, Spiral Computed

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1513041
UMLS CUI [1,2]
C0439534
UMLS CUI [1,3]
C1265611
UMLS CUI [2,1]
C0221198
UMLS CUI [2,2]
C0552406
UMLS CUI [3,1]
C0242485
UMLS CUI [3,2]
C0439858
UMLS CUI [4]
C0860888
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
any prior radiation therapy to the thoracic area.
Beschreibung

History of radiation therapy to chest

Datentyp

boolean

Alias
UMLS CUI [1]
C4038799
active and ongoing systemic infection.
Beschreibung

Sepsis

Datentyp

boolean

Alias
UMLS CUI [1]
C0243026
prior radiation to greater than 25% of the bone marrow.
Beschreibung

prior radiation therapy Bone Marrow Percentage

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0279134
UMLS CUI [1,2]
C0005953
UMLS CUI [1,3]
C0439165
ecog ps other than 2
Beschreibung

ECOG performance status

Datentyp

boolean

Alias
UMLS CUI [1]
C1520224
patients with a known hypersensitivity to gemcitabine and carboplatin.
Beschreibung

Hypersensitivity gemcitabine | Hypersensitivity Carboplatin

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0045093
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0079083
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Ähnliche Modelle

Eligibility Non-Small Cell Lung Cancer NCT00190710

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Non-Small Cell Lung Carcinoma | TNM clinical staging | Pleural effusion disorder | Pericardial effusion
Item
histologic or cytologic new diagnosis of nsclc, stage iiib with a cytologically positive pleural or pericardial effusion or stage iv.
boolean
C0007131 (UMLS CUI [1])
C3258246 (UMLS CUI [2])
C0032227 (UMLS CUI [3])
C0031039 (UMLS CUI [4])
Prior Chemotherapy Non-Small Cell Lung Carcinoma | Adjuvant therapy Non-Small Cell Lung Carcinoma | Neoadjuvant Therapy Non-Small Cell Lung Carcinoma
Item
no prior chemotherapy, including adjuvant or neoadjuvant therapy, for the treatment of nsclc.
boolean
C1514457 (UMLS CUI [1,1])
C0007131 (UMLS CUI [1,2])
C0677850 (UMLS CUI [2,1])
C0007131 (UMLS CUI [2,2])
C0600558 (UMLS CUI [3,1])
C0007131 (UMLS CUI [3,2])
ECOG performance status
Item
ecog performance status of 2 .
boolean
C1520224 (UMLS CUI [1])
major surgery | Operative Surgical Procedures | Mediastinoscopy | Thoracoscopy | Thoracostomy
Item
patients must be at least 3 weeks since major surgery. patients must be at least 1 week since surgery, such as mediastinoscopy, pleuroscopy, or thoracostomy.
boolean
C0679637 (UMLS CUI [1])
C0543467 (UMLS CUI [2])
C0025065 (UMLS CUI [3])
C0039989 (UMLS CUI [4])
C0039990 (UMLS CUI [5])
Measurable Disease Dimensions Quantity | Lesion Longest Diameter | Measurement technique conventional | Tomography, Spiral Computed
Item
patients must have measurable disease, defined as lesions that can be accurately measured in at least 1 dimension (longest diameter to be recorded) as greater than or equal to 20 mm with conventional techniques or as greater than 10 mm with spiral ct scan.
boolean
C1513041 (UMLS CUI [1,1])
C0439534 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0221198 (UMLS CUI [2,1])
C0552406 (UMLS CUI [2,2])
C0242485 (UMLS CUI [3,1])
C0439858 (UMLS CUI [3,2])
C0860888 (UMLS CUI [4])
Item Group
C0680251 (UMLS CUI)
History of radiation therapy to chest
Item
any prior radiation therapy to the thoracic area.
boolean
C4038799 (UMLS CUI [1])
Sepsis
Item
active and ongoing systemic infection.
boolean
C0243026 (UMLS CUI [1])
prior radiation therapy Bone Marrow Percentage
Item
prior radiation to greater than 25% of the bone marrow.
boolean
C0279134 (UMLS CUI [1,1])
C0005953 (UMLS CUI [1,2])
C0439165 (UMLS CUI [1,3])
ECOG performance status
Item
ecog ps other than 2
boolean
C1520224 (UMLS CUI [1])
Hypersensitivity gemcitabine | Hypersensitivity Carboplatin
Item
patients with a known hypersensitivity to gemcitabine and carboplatin.
boolean
C0020517 (UMLS CUI [1,1])
C0045093 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0079083 (UMLS CUI [2,2])
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