Information:
Fel:
ID
41193
Beskrivning
NSCLC Burden of Illness Study; ODM derived from: https://clinicaltrials.gov/show/NCT01772225
Länk
https://clinicaltrials.gov/show/NCT01772225
Nyckelord
Versioner (1)
- 2020-07-10 2020-07-10 -
Rättsinnehavare
See clinicaltrials.gov
Uppladdad den
10 juli 2020
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Lung Cancer, Non-Small Cell NCT01772225
Eligibility Lung Cancer, Non-Small Cell NCT01772225
- StudyEvent: Eligibility
Similar models
Eligibility Lung Cancer, Non-Small Cell NCT01772225
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Patients Medical Records
Item
patient medical records will be screened using the following criteria:
boolean
C0030705 (UMLS CUI [1,1])
C0025102 (UMLS CUI [1,2])
C0025102 (UMLS CUI [1,2])
Age | Non-Small Cell Lung Carcinoma TNM clinical staging
Item
patients must be aged 18 years or older at the time of first presentation with clinical stage ib-iiia nsclc.
boolean
C0001779 (UMLS CUI [1])
C0007131 (UMLS CUI [2,1])
C3258246 (UMLS CUI [2,2])
C0007131 (UMLS CUI [2,1])
C3258246 (UMLS CUI [2,2])
Complete excision Non-Small Cell Lung Carcinoma TNM clinical staging | Investigator Primary Care Provider
Item
patients must have complete resection of pathologic stage ib-iiia nsclc at least 1 calendar month prior to the date of screening, according to the current classification recommended by the international association for the study of lung cancer (2009). the investigator/study site must have been the main care provider for the patient during the period of treatment or management of the patient's nsclc.
boolean
C0015250 (UMLS CUI [1,1])
C0007131 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,3])
C0035173 (UMLS CUI [2,1])
C1547431 (UMLS CUI [2,2])
C0007131 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,3])
C0035173 (UMLS CUI [2,1])
C1547431 (UMLS CUI [2,2])
Wedge resection
Item
patients who underwent wedge resection.
boolean
C0184909 (UMLS CUI [1])
Excision Recent | Systemic Therapy Adjuvant Type Unknown
Item
patients whose resection was less than 1 calendar month before the date of screening. patients who received adjuvant systemic treatment within a clinical trial if the type of adjuvant treatment is either unknown or is not recommended by international clinical guidelines [european society for medical oncology (esmo), national comprehensive cancer network (nccn)].
boolean
C0728940 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
C1515119 (UMLS CUI [2,1])
C1522673 (UMLS CUI [2,2])
C0332307 (UMLS CUI [2,3])
C0439673 (UMLS CUI [2,4])
C0332185 (UMLS CUI [1,2])
C1515119 (UMLS CUI [2,1])
C1522673 (UMLS CUI [2,2])
C0332307 (UMLS CUI [2,3])
C0439673 (UMLS CUI [2,4])
Patient unavailable Follow-up
Item
patients who are lost to follow-up:
boolean
C1301818 (UMLS CUI [1,1])
C3274571 (UMLS CUI [1,2])
C3274571 (UMLS CUI [1,2])
Patient care Study Site Discontinued | Patients Contact Discontinued
Item
living patients who are no longer under the care of the site or can no longer be contacted.
boolean
C0017313 (UMLS CUI [1,1])
C2825164 (UMLS CUI [1,2])
C1444662 (UMLS CUI [1,3])
C0030705 (UMLS CUI [2,1])
C0332158 (UMLS CUI [2,2])
C1444662 (UMLS CUI [2,3])
C2825164 (UMLS CUI [1,2])
C1444662 (UMLS CUI [1,3])
C0030705 (UMLS CUI [2,1])
C0332158 (UMLS CUI [2,2])
C1444662 (UMLS CUI [2,3])
Patient Deceased
Item
deceased patients who were transferred to another nsclc treatment centre before death.
boolean
C1555024 (UMLS CUI [1])
Treatment Cancer Other
Item
patients with concomitant malignancies who received treatment for other cancers at any time during their treatment or follow-up for nsclc.
boolean
C0087111 (UMLS CUI [1,1])
C1707251 (UMLS CUI [1,2])
C1707251 (UMLS CUI [1,2])