Informations:
Erreur:
ID
21533
Description
Bevacizumab and Carboplatin/Paclitaxel and Radiation in Non-Small Cell Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00578149
Lien
https://clinicaltrials.gov/show/NCT00578149
Mots-clés
Versions (1)
- 26/04/2017 26/04/2017 -
Téléchargé le
26 avril 2017
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
Modèle Commentaires :
Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.
Groupe Item commentaires pour :
Item commentaires pour :
Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.
Eligibility Non-Small Cell Lung Cancer NCT00578149
Eligibility Non-Small Cell Lung Cancer NCT00578149
- StudyEvent: Eligibility
Similar models
Eligibility Non-Small Cell Lung Cancer NCT00578149
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Non-small cell lung cancer, operability, tumor stage
Item
histologically confirmed non-small cell lung cancer (nsclc) that have been evaluated and determined not to be candidates for surgical resection as part of their definitive management of stage iii disease.
boolean
C0007131 (UMLS CUI [1])
C0205188 (UMLS CUI [2])
C1300072 (UMLS CUI [3])
C0205188 (UMLS CUI [2])
C1300072 (UMLS CUI [3])
Age
Item
age 18 years or older
boolean
C0001779 (UMLS CUI [1])
ECOG Performance Status
Item
ecog performance status of 0-1
boolean
C1520224 (UMLS CUI [1])
Life Expectancy
Item
life expectancy of greater than six months
boolean
C0023671 (UMLS CUI [1])
Organ and bone marrow function
Item
normal organ and marrow function
boolean
C0678852 (UMLS CUI [1])
C0005953 (UMLS CUI [2])
C0005953 (UMLS CUI [2])
Contraceptive methods
Item
women and men of child-bearing potential must agree to use adequate contraception
boolean
C0700589 (UMLS CUI [1])
Prior Chemotherapy or Radiation
Item
prior chemotherapy or thoracic radiation therapy
boolean
C0279134 (UMLS CUI [1])
C1514457 (UMLS CUI [2])
C1514457 (UMLS CUI [2])
Histological finding and tumor site
Item
squamous histology or any histology in close proximity to a major vessel
boolean
C0449575 (UMLS CUI [1])
C0475445 (UMLS CUI [2])
C0475445 (UMLS CUI [2])
Hemoptysis
Item
active hemoptysis
boolean
C0019079 (UMLS CUI [1])
Hypercoagulability
Item
history of hypercoagulability
boolean
C0398623 (UMLS CUI [1])
Metastatic disease
Item
known distant metastatic disease
boolean
C0027627 (UMLS CUI [1])
Hypersensitivity to bevacizumab, carboplatin, paclitaxel or other agents used in this study
Item
history of allergic reactions attributed to compounds with similar chemical or biological composition to bevacizumab, carboplatin, paclitaxel or other agents used in this study
boolean
C0020517 (UMLS CUI [1,1])
C0796392 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0079083 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0144576 (UMLS CUI [3,2])
C0020517 (UMLS CUI [4,1])
C0304229 (UMLS CUI [4,2])
C0796392 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0079083 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0144576 (UMLS CUI [3,2])
C0020517 (UMLS CUI [4,1])
C0304229 (UMLS CUI [4,2])
Comorbidity
Item
patients with uncontrolled intercurrent illness
boolean
C0009488 (UMLS CUI [1])
Pregnancy
Item
pregnant women
boolean
C0032961 (UMLS CUI [1])
Major surgical procedure, open biopsy, or significant traumatic injury
Item
major surgical procedure, open biopsy, or significant traumatic injury with in 28 days prior to day 0
boolean
C0543467 (UMLS CUI [1])
C0184922 (UMLS CUI [2])
C3263723 (UMLS CUI [3])
C0184922 (UMLS CUI [2])
C3263723 (UMLS CUI [3])
Minor surgical procedure
Item
minor surgical procedure within 7 days to day 0
boolean
C0038904 (UMLS CUI [1])
HIV therapy
Item
hiv-positive patients receiving combination anti-retroviral therapy.
boolean
C0920551 (UMLS CUI [1])
Prior malignancy
Item
non-skin cancer malignancy in the past 5 years.
boolean
C2735088 (UMLS CUI [1])