Information:
Fel:
ID
31161
Beskrivning
Gemcitabine and Carboplatin for Elderly Patient With Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00881296
Länk
https://clinicaltrials.gov/show/NCT00881296
Nyckelord
Versioner (1)
- 2018-07-24 2018-07-24 -
Rättsinnehavare
See clinicaltrials.gov
Uppladdad den
24 juli 2018
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Non-Small Cell Lung Cancer NCT00881296
Eligibility Non-Small Cell Lung Cancer NCT00881296
- StudyEvent: Eligibility
Similar models
Eligibility Non-Small Cell Lung Cancer NCT00881296
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Non-Small Cell Lung Carcinoma TNM clinical staging
Item
diagnosis of histologically confirmed stage iiib or iv non-small cell lung cancer
boolean
C0007131 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,2])
ECOG performance status
Item
good performance status (ecog 0-1)
boolean
C1520224 (UMLS CUI [1])
Prior Therapy Absent
Item
no previous treatment
boolean
C1514463 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,2])
Age
Item
age 76 years and older
boolean
C0001779 (UMLS CUI [1])
Bone Marrow function | Liver function | Renal function
Item
adequate bone marrow, liver and renal functions
boolean
C0005953 (UMLS CUI [1,1])
C0031843 (UMLS CUI [1,2])
C0232741 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
C0031843 (UMLS CUI [1,2])
C0232741 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
Pregnancy Absent
Item
no pregnant
boolean
C0032961 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,2])
Measurable Disease | Lesion Quantity | Longest Diameter Spiral CT scan
Item
measurable disease, defined as at least one lesion whose longest diameter can be accurately measured as >=1.0 cm by spiral ct scan
boolean
C1513041 (UMLS CUI [1])
C0221198 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0552406 (UMLS CUI [3,1])
C0860888 (UMLS CUI [3,2])
C0221198 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0552406 (UMLS CUI [3,1])
C0860888 (UMLS CUI [3,2])
Informed Consent
Item
provided written informed consent
boolean
C0021430 (UMLS CUI [1])
Severe medical complication | Cancer Other
Item
severe complications or a concomitant malignancy
boolean
C3495031 (UMLS CUI [1])
C1707251 (UMLS CUI [2])
C1707251 (UMLS CUI [2])
Therapeutic radiology procedure | Chemotherapy | Immunotherapy | Epidermal growth factor receptor inhibitor
Item
prior and other concurrent radiotherapy, chemotherapy, immunotherapy, egfr tyrosine kinase inhibitors
boolean
C1522449 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
C0021083 (UMLS CUI [3])
C1443775 (UMLS CUI [4])
C0392920 (UMLS CUI [2])
C0021083 (UMLS CUI [3])
C1443775 (UMLS CUI [4])
Pneumonia, Interstitial | Pulmonary Fibrosis
Item
interstitial pneumonia or lung fibrosis
boolean
C0206061 (UMLS CUI [1])
C0034069 (UMLS CUI [2])
C0034069 (UMLS CUI [2])
Medical contraindication Gemcitabine | Medical contraindication Carboplatin
Item
contraindicated gemcitabine or carboplatin
boolean
C1301624 (UMLS CUI [1,1])
C0045093 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0079083 (UMLS CUI [2,2])
C0045093 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0079083 (UMLS CUI [2,2])
Study Subject Participation Status Inappropriate
Item
inappropriate patients for entry to this study, judged by the physicians
boolean
C2348568 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
C1548788 (UMLS CUI [1,2])