Informatie:
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ID
16671
Beschrijving
An Open, Randomized, Multicentre, Phase II Pilot Study; ODM derived from: https://clinicaltrials.gov/show/NCT00293085
Link
https://clinicaltrials.gov/show/NCT00293085
Trefwoorden
Versies (1)
- 31-07-16 31-07-16 -
Geüploaded op
31 juli 2016
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Non-Small Cell Lung Cancer NCT00293085
Eligibility Non-Small Cell Lung Cancer NCT00293085
- StudyEvent: Eligibility
Similar models
Eligibility Non-Small Cell Lung Cancer NCT00293085
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
nsclc stage
Item
histologically documented nsclc stage i-ii
boolean
C0278504 (UMLS CUI [1])
C0278505 (UMLS CUI [2])
C0278505 (UMLS CUI [2])
r0 resection
Item
complete resection of tumor amd resection margins microscopically tumor free.
boolean
C0015250 (UMLS CUI [1])
lobectomy, bilobectomy or pneumectomy
Item
surgical procedure: according to necessity for oncology radicality a lobectomy, bilobectomy or pneumectomy will be performed with either radical mediastinal lymphadenectomy or complete sampling of all relevant lymph node areas.
boolean
C0023928 (UMLS CUI [1])
C0396580 (UMLS CUI [2])
C0032284 (UMLS CUI [3])
C0396580 (UMLS CUI [2])
C0032284 (UMLS CUI [3])
randomization within 60 days after surgical required.
Item
randomization within 60 days after surgical required.
boolean
C0034656 (UMLS CUI [1,1])
C0032790 (UMLS CUI [1,2])
C0032790 (UMLS CUI [1,2])
ID.5
Item
initial work-up
boolean
general conditions
Item
general conditions: 19-70 years, who performance status 0-2, adequate hematological function, adequate renal and hepatic function, negative pregnancy test.
boolean
C0001779 (UMLS CUI [1])
C1298651 (UMLS CUI [2])
C0678852 (UMLS CUI [3])
C0427780 (UMLS CUI [4])
C1298651 (UMLS CUI [2])
C0678852 (UMLS CUI [3])
C0427780 (UMLS CUI [4])
nsclc stage ii-iv, sclc or alveolar carcinoma
Item
nsclc stage ii-iv, sclc or alveolar carcinoma
boolean
C0278506 (UMLS CUI [1])
C0278987 (UMLS CUI [2])
C0149925 (UMLS CUI [3])
C0007120 (UMLS CUI [4])
C0278987 (UMLS CUI [2])
C0149925 (UMLS CUI [3])
C0007120 (UMLS CUI [4])
cns metastases
Item
clinical evidence of cns metastases
boolean
C0686377 (UMLS CUI [1])
pregnant and lactating
Item
pregnant and lactating patients
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
C0006147 (UMLS CUI [1,2])
past or concurrent history of malignancies
Item
past or concurrent history of malignancies other than nsclc,except for curatively treated non melanoma of the skin or in situ cervical carcinoma or other curatively treated cancer with no evidence of disease for at least five years.
boolean
C0006826 (UMLS CUI [1])
prior or concurrent antitumor therapy for nsclc other than surgery
Item
prior or concurrent antitumor therapy for nsclc other than surgery.
boolean
C1522449 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
C0392920 (UMLS CUI [2])
clinical trial participation status
Item
concomitant participation in clinical studies of non-approved experimental agents or procedures.
boolean
C2348568 (UMLS CUI [1])
major complications after surgery
Item
major complications after surgery
boolean
C0032787 (UMLS CUI [1])
comorbidity
Item
serious concomitant medical conditions
boolean
C0009488 (UMLS CUI [1])
study compliance
Item
psychological,familial, sociological or geographical conditions which do not permit compliance with the study protocol
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0348080 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,2])
C0348080 (UMLS CUI [1,3])