Informatie:
Fout:
ID
22114
Beschrijving
Survival Study of Docetaxel and Carboplatin as Neo-Adjuvant Vs Adjuvant Chemotherapy in Early Stage NSLC; ODM derived from: https://clinicaltrials.gov/show/NCT00321334
Link
https://clinicaltrials.gov/show/NCT00321334
Trefwoorden
Versies (1)
- 20-05-17 20-05-17 -
Geüploaded op
20 mei 2017
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Non-small Cell Lung Cancer NCT00321334
Eligibility Non-small Cell Lung Cancer NCT00321334
- StudyEvent: Eligibility
Similar models
Eligibility Non-small Cell Lung Cancer NCT00321334
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Non-Small Cell Lung Carcinoma TNM clinical staging | Chemotherapy Absent | Therapeutic radiology procedure Absent | Targeted Therapy Absent
Item
histologically or cytologically confirmed stage ib-iiia non-small cell lung cancer patients,without previous chemotherapy, radiotherapy or target-therapy;
boolean
C0007131 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
C0392920 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C1522449 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
C2985566 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
C3258246 (UMLS CUI [1,2])
C0392920 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C1522449 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
C2985566 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
Age
Item
age from 18 to 75;
boolean
C0001779 (UMLS CUI [1])
ECOG performance status
Item
ps with ecoc 0-1;
boolean
C1520224 (UMLS CUI [1])
Hematologic function | Liver function | Renal function
Item
adequate haematological and hepatic- renal function;
boolean
C0221130 (UMLS CUI [1])
C0232741 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
C0232741 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
Life Expectancy
Item
expected to live longer than 12 months;
boolean
C0023671 (UMLS CUI [1])
Informed Consent
Item
the informed consent should be signed.
boolean
C0021430 (UMLS CUI [1])
Small cell carcinoma of lung
Item
patients with small cell lung cancer;
boolean
C0149925 (UMLS CUI [1])
cancer treatment
Item
already receiving any prior anti-cancer treatment;
boolean
C0920425 (UMLS CUI [1])
Pregnancy
Item
pregnant women;
boolean
C0032961 (UMLS CUI [1])
Diabetic - poor control | Mental disorder
Item
uncontrolled diabetes, mental disease;
boolean
C0421258 (UMLS CUI [1])
C0004936 (UMLS CUI [2])
C0004936 (UMLS CUI [2])
Liver Failure | Kidney Failure
Item
hepatic and renal function failure;
boolean
C0085605 (UMLS CUI [1])
C0035078 (UMLS CUI [2])
C0035078 (UMLS CUI [2])
Study Subject Participation Status Inappropriate
Item
the investigators believe the patient is not suitable to be enrolled in the study
boolean
C2348568 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
C1548788 (UMLS CUI [1,2])