Informationen:
Fehler:
ID
36589
Beschreibung
An International Study on the Use of PET/CT in Radiotherapy Planning in Low and Middle Income Countries; ODM derived from: https://clinicaltrials.gov/show/NCT02247713
Link
https://clinicaltrials.gov/show/NCT02247713
Stichworte
Versionen (1)
- 23.05.19 23.05.19 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
23. Mai 2019
DOI
Für eine Beantragung loggen Sie sich ein.
Lizenz
Creative Commons BY 4.0
Modell Kommentare :
Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.
Itemgroup Kommentare für :
Item Kommentare für :
Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.
Eligibility Non Small Cell Lung Cancer Stage III NCT02247713
Eligibility Non Small Cell Lung Cancer Stage III NCT02247713
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Non Small Cell Lung Cancer Stage III NCT02247713
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Non-Small Cell Lung Carcinoma
Item
pathologically confirmed nsclc
boolean
C0007131 (UMLS CUI [1])
TNM clinical staging
Item
stage iii as per local diagnostic protocol or agreement of local multidisciplinary team
boolean
C3258246 (UMLS CUI [1])
Patient Available Follow-up
Item
available for clinical follow-up for at least 2 years
boolean
C0030705 (UMLS CUI [1,1])
C0470187 (UMLS CUI [1,2])
C3274571 (UMLS CUI [1,3])
C0470187 (UMLS CUI [1,2])
C3274571 (UMLS CUI [1,3])
Patient suitable Therapeutic procedure | Target Volume Radical
Item
suitable for treatment with a radical target volume in the opinion of a radiation oncologist
boolean
C0030705 (UMLS CUI [1,1])
C3900053 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
C1521840 (UMLS CUI [2,1])
C0449468 (UMLS CUI [2,2])
C0439807 (UMLS CUI [2,3])
C3900053 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
C1521840 (UMLS CUI [2,1])
C0449468 (UMLS CUI [2,2])
C0439807 (UMLS CUI [2,3])
ECOG performance status
Item
ecog performance 0 or 1
boolean
C1520224 (UMLS CUI [1])
Informed Consent
Item
signed informed consent
boolean
C0021430 (UMLS CUI [1])
Ability Commence Therapeutic radiology procedure | Radiotherapy planning PET/CT
Item
ability to commence radiation therapy within 4 weeks of acquisition of the rtp pet/ct
boolean
C0085732 (UMLS CUI [1,1])
C3274784 (UMLS CUI [1,2])
C1522449 (UMLS CUI [1,3])
C0454111 (UMLS CUI [2,1])
C1699633 (UMLS CUI [2,2])
C3274784 (UMLS CUI [1,2])
C1522449 (UMLS CUI [1,3])
C0454111 (UMLS CUI [2,1])
C1699633 (UMLS CUI [2,2])
Patient suitable Chemoradiotherapy
Item
suitable for concurrent chemoradiotherapy (prospective cohort only)
boolean
C0030705 (UMLS CUI [1,1])
C3900053 (UMLS CUI [1,2])
C0436307 (UMLS CUI [1,3])
C3900053 (UMLS CUI [1,2])
C0436307 (UMLS CUI [1,3])
Cancer Other | Exception Skin carcinoma
Item
other neoplasms in the last 5 years except non-melanoma skin cancer
boolean
C1707251 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0699893 (UMLS CUI [2,2])
C1705847 (UMLS CUI [2,1])
C0699893 (UMLS CUI [2,2])
TNM clinical staging
Item
stage iv disease diagnosed before acquisition of staging pet/ct
boolean
C3258246 (UMLS CUI [1])
Informed Consent Unable
Item
inability to provide informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,2])
Diabetic - poor control
Item
uncontrolled diabetes mellitus
boolean
C0421258 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnant or breast feeding mothers
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Tuberculosis
Item
tuberculosis
boolean
C0041296 (UMLS CUI [1])
Chemotherapy Neoadjuvant
Item
neo-adjuvant chemotherapy
boolean
C0392920 (UMLS CUI [1,1])
C1298676 (UMLS CUI [1,2])
C1298676 (UMLS CUI [1,2])