Informatie:
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ID
13077
Beschrijving
LIFE-Lung Bronchoscopy in Patients at Risk for Developing Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00260598
Link
https://clinicaltrials.gov/show/NCT00260598
Trefwoorden
Versies (1)
- 15-01-16 15-01-16 -
Houder van rechten
CC BY-NC 3.0
Geüploaded op
15 januari 2016
DOI
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Licentie
Creative Commons BY-NC 3.0
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Eligibility Non-Small-Cell Lung Carcinoma NCT00260598
Eligibility Non-Small-Cell Lung Carcinoma NCT00260598
- StudyEvent: Eligibility
Similar models
Eligibility Non-Small-Cell Lung Carcinoma NCT00260598
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
non small cell lung cancer
Item
persons with non-small cell lung cancer (nsclc) who have undergone surgical resection, via a lobectomy, pneumonectomy, or wedge resection and currently have no evidence of disease (ned).
boolean
C0007131 (UMLS CUI [1])
head/neck squamous cell cancer
Item
persons with head/neck squamous cell cancer who have undergone radical head and/or neck resection and who currently have ned.
boolean
C0007137 (UMLS CUI [1])
chronic obstructive pulmonary disease
Item
persons with severe chronic, obstructive, pulmonary disease as evidenced by pulmonary function abnormalities: i.e. fev1 < 50%predicted; rv > 200% predicted and/or dlco < 40% predicted.
boolean
C0024117 (UMLS CUI [1])
hypertension
Item
persons with uncontrolled hypertension (systolic pressure >200mmhg, diastolic pressure >120 mm hg)
boolean
C0020538 (UMLS CUI [1])
unstable angina
Item
persons with unstable angina.
boolean
C0002965 (UMLS CUI [1])
pneumonia
Item
persons with known or suspected pneumonia.
boolean
C0032285 (UMLS CUI [1])
bronchitis
Item
persons with acute bronchitis within one month of the procedure.
boolean
C0006277 (UMLS CUI [1])
chemotherapy, radiotherapy
Item
persons who have received neoadjuvant or adjuvant chemo- or radio-therapy within the past six months.
boolean
C0392920 (UMLS CUI [1])
C1522449 (UMLS CUI [2])
C1522449 (UMLS CUI [2])
Leukocytes, platelets
Item
persons with white blood count (wbc) less than 2000 or greater than 20,000 and/or platelet count less than 50,000.
boolean
C0023508 (UMLS CUI [1])
C0032181 (UMLS CUI [2])
C0032181 (UMLS CUI [2])
bleeding disorder
Item
persons with any known bleeding dyscrasia.
boolean
C0005779 (UMLS CUI [1])
photosensitizing drugs
Item
persons who have received fluorescent photosensitizing drugs such as photofrin within one month of the procedure.
boolean
C0162713 (UMLS CUI [1])
allergic reaction to topical xylocaine
Item
persons with a known allergic reaction to topical xylocaine (lidocaine).
boolean
C0020517 (UMLS CUI [1,1])
C0023660 (UMLS CUI [1,2])
C0023660 (UMLS CUI [1,2])
chemopreventive drugs
Item
persons who have received or are on chemopreventive drugs (i.e. retinoic acid) within one month of the procedure.
boolean
C1516463 (UMLS CUI [1])
radiotherapy
Item
persons who have received ionizing radiation to the chest within six months of the procedure.
boolean
C1522449 (UMLS CUI [1])
chemotherapy
Item
persons who have received systemic cytotoxic chemotherapeutic agents within the past six months.
boolean
C0392920 (UMLS CUI [1])
pregnancy
Item
persons who are pregnant or nursing. all women of childbearing potential must have a negative serum pregnancy test prior to enrollment.
boolean
C0032961 (UMLS CUI [1])