Informatie:
Fout:
ID
13147
Beschrijving
Preoperative or Postoperative Therapy of Patients With Stages IB, II, IIIA Non-Small Cell Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00193310
Link
https://clinicaltrials.gov/show/NCT00193310
Trefwoorden
Versies (1)
- 19-01-16 19-01-16 -
Geüploaded op
19 januari 2016
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Lung Cancer NCT00193310
Eligibility Lung Cancer NCT00193310
- StudyEvent: Eligibility
Similar models
Eligibility Lung Cancer NCT00193310
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
non-small cell lung cancer
Item
non-small cell lung cancer
boolean
C0007131 (UMLS CUI [1])
neoadjuvant therapy
Item
neoadjuvant candidates must have potentially resectable disease
boolean
C0600558 (UMLS CUI [1])
C0015250 (UMLS CUI [2])
C0015250 (UMLS CUI [2])
adjuvant therapy
Item
adjuvant candidates must have had complete resection
boolean
C0677850 (UMLS CUI [1])
C0015250 (UMLS CUI [2])
C0015250 (UMLS CUI [2])
tumor stage
Item
clinical stage ib, ii, or iiia non-small cell lung cancer
boolean
C1300072 (UMLS CUI [1])
ecog
Item
ecog performance status 0 or 1
boolean
C1520224 (UMLS CUI [1])
bone marrow, liver and kidney function
Item
adequate bone marrow, liver and kidney function
boolean
C0232741 (UMLS CUI [1])
C0005953 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
C0005953 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
chemotherapy, radiotherapy
Item
no previous chemotherapy or radiation therapy for non-small cell lung cancer.
boolean
C0392920 (UMLS CUI [1,1])
C1522449 (UMLS CUI [1,2])
C1522449 (UMLS CUI [1,2])
informed consent
Item
give written informed consent.
boolean
C0021430 (UMLS CUI [1])
tumor stage
Item
stage iiia with n2 nodes > 6 cm
boolean
C1300072 (UMLS CUI [1])
tumor stage
Item
stage iiib or iv disease
boolean
C1300072 (UMLS CUI [1])
age
Item
age <18 years
boolean
C0001779 (UMLS CUI [1])
ecog
Item
ecog performance status 2 or higher
boolean
C1520224 (UMLS CUI [1])
health status, inoperable
Item
considered inoperable based on general medical condition
boolean
C0018759 (UMLS CUI [1,1])
C0205187 (UMLS CUI [1,2])
C0205187 (UMLS CUI [1,2])
malignancy
Item
history of prior malignancy within five years
boolean
C0006826 (UMLS CUI [1])
pregnancy, lactation
Item
women who are pregnant or lactating
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
C0006147 (UMLS CUI [1,2])
additional criteria
Item
please note: there are additional inclusion/exclusion criteria. the study center will determine if you meet all of the criteria. if you do not qualify for the trial, study personnel will explain the reasons. if you do qualify, study personnel will explain the trial in detail and answer any questions you may have.
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