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ID
36584
Beschrijving
Isotoxic Intensity Modulated Radiotherapy (IMRT) in Stage III Non Small Cell Lung Cancer (NSCLC) - A Feasibility Study; ODM derived from: https://clinicaltrials.gov/show/NCT01836692
Link
https://clinicaltrials.gov/show/NCT01836692
Trefwoorden
Versies (1)
- 23-05-19 23-05-19 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
23 mei 2019
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Non Small Cell Lung Cancer NCT01836692
Eligibility Non Small Cell Lung Cancer NCT01836692
- StudyEvent: Eligibility
Similar models
Eligibility Non Small Cell Lung Cancer NCT01836692
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Non-Small Cell Lung Carcinoma
Item
histologically or cytologically confirmed nsclc
boolean
C0007131 (UMLS CUI [1])
Disease Inoperable TNM clinical staging | PET scan | Mediastinoscopy | Thoracoscopy
Item
inoperable stage iii disease (t3n1-3, any t4, any n2 -3) confirmed by pet scanning, mediastinoscopy or thoracoscopy
boolean
C0012634 (UMLS CUI [1,1])
C0205187 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,3])
C0032743 (UMLS CUI [2])
C0025065 (UMLS CUI [3])
C0039989 (UMLS CUI [4])
C0205187 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,3])
C0032743 (UMLS CUI [2])
C0025065 (UMLS CUI [3])
C0039989 (UMLS CUI [4])
Chemotherapy cycle Platinum-Based Quantity | Therapeutic radiology procedure
Item
patients treated with at least 2 cycles of platinum based induction chemotherapy and able to start radiotherapy within 5 weeks of the last cycle of chemotherapy
boolean
C1302181 (UMLS CUI [1,1])
C1514162 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C1522449 (UMLS CUI [2])
C1514162 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C1522449 (UMLS CUI [2])
Neoplasm Inoperable
Item
tumour judged inoperable by a lung mdt
boolean
C0027651 (UMLS CUI [1,1])
C0205187 (UMLS CUI [1,2])
C0205187 (UMLS CUI [1,2])
Age
Item
age 18+, no upper age limit
boolean
C0001779 (UMLS CUI [1])
ECOG performance status
Item
performance status (ps) - ecog 0-2. patients with ps 2 whose general condition is explained by disease can be included at the discretion of the local investigator. patients with ps 2 as a result of co-morbid conditions will be excluded
boolean
C1520224 (UMLS CUI [1])
Appropriateness Therapeutic radiology procedure Radical
Item
patient considered suitable for radical rt
boolean
C0814634 (UMLS CUI [1,1])
C1522449 (UMLS CUI [1,2])
C0439807 (UMLS CUI [1,3])
C1522449 (UMLS CUI [1,2])
C0439807 (UMLS CUI [1,3])
Therapeutic radiology procedure Radical Neoplasm
Item
tumour that can be encompassed within a radical rt treatment volume (mld expected to be <20gy)
boolean
C1522449 (UMLS CUI [1,1])
C0439807 (UMLS CUI [1,2])
C0027651 (UMLS CUI [1,3])
C0439807 (UMLS CUI [1,2])
C0027651 (UMLS CUI [1,3])
Appropriateness Concurrent Chemoradiotherapy
Item
patients suitable for standard concurrent ctrt
boolean
C0814634 (UMLS CUI [1,1])
C3178775 (UMLS CUI [1,2])
C3178775 (UMLS CUI [1,2])
Appropriateness Therapeutic radiology procedure Radical | Etiology Performance status | Etiology Comorbidity
Item
patients only suitable for radical rt due to ps and co-morbidities
boolean
C0814634 (UMLS CUI [1,1])
C1522449 (UMLS CUI [1,2])
C0439807 (UMLS CUI [1,3])
C0015127 (UMLS CUI [2,1])
C1518965 (UMLS CUI [2,2])
C0015127 (UMLS CUI [3,1])
C0009488 (UMLS CUI [3,2])
C1522449 (UMLS CUI [1,2])
C0439807 (UMLS CUI [1,3])
C0015127 (UMLS CUI [2,1])
C1518965 (UMLS CUI [2,2])
C0015127 (UMLS CUI [3,1])
C0009488 (UMLS CUI [3,2])