Informations:
Erreur:
ID
27399
Description
Erlotinib Concurrent With Radiation Therapy in Non-small-cell Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00973310
Lien
https://clinicaltrials.gov/show/NCT00973310
Mots-clés
Versions (1)
- 13/11/2017 13/11/2017 -
Détendeur de droits
See clinicaltrials.gov
Téléchargé le
13 novembre 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 Carcinoma, Non-Small Cell Lung NCT00973310
Eligibility Carcinoma, Non-Small Cell Lung NCT00973310
- StudyEvent: Eligibility
Similar models
Eligibility Carcinoma, Non-Small Cell Lung NCT00973310
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Age
Item
aged 18-70 years，
boolean
C0001779 (UMLS CUI [1])
Non-Small Cell Lung Carcinoma TNM clinical staging
Item
patients with stage iiia-iiib nsclc
boolean
C0007131 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,2])
Hematologic function | White Blood Cell Count procedure | Platelet Count measurement | Liver function | Serum total bilirubin measurement | Renal function | Creatinine clearance measurement
Item
adequate hematologic (wbc and platelet counts within normal limits), hepatic (total bilirubin level <= two times the upper limit of normal), and renal (creatinine clearance >= 50ml/min) functions
boolean
C0221130 (UMLS CUI [1])
C0023508 (UMLS CUI [2])
C0032181 (UMLS CUI [3])
C0232741 (UMLS CUI [4])
C1278039 (UMLS CUI [5])
C0232804 (UMLS CUI [6])
C0373595 (UMLS CUI [7])
C0023508 (UMLS CUI [2])
C0032181 (UMLS CUI [3])
C0232741 (UMLS CUI [4])
C1278039 (UMLS CUI [5])
C0232804 (UMLS CUI [6])
C0373595 (UMLS CUI [7])
Chemotherapy Absent | Chemotherapy cycle Neoadjuvant Quantity
Item
no history of chemotherapy or less than 4 cycles neoadjuvant chemotherapy
boolean
C0392920 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C1302181 (UMLS CUI [2,1])
C0600558 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
C0332197 (UMLS CUI [1,2])
C1302181 (UMLS CUI [2,1])
C0600558 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
Intolerance Chemoradiotherapy | Chemoradiotherapy Refused
Item
can not tolerate or refuse concurrent chemoradiotherapy
boolean
C0231199 (UMLS CUI [1,1])
C0436307 (UMLS CUI [1,2])
C0436307 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
C0436307 (UMLS CUI [1,2])
C0436307 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
Radiotherapy to thorax Absent
Item
no history of thoracic rt
boolean
C4038705 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,2])
Informed Consent
Item
written informed consent obtained
boolean
C0021430 (UMLS CUI [1])
Cancer Other
Item
with other malignancy
boolean
C1707251 (UMLS CUI [1])
Cardiopulmonary disease Severe
Item
with severe cardiopulmonary disease
boolean
C0034072 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,2])
Liver Dysfunction | Renal function | Intolerance Combined Modality Therapy
Item
compromised liver or renal function that could not tolerate the combined therapy
boolean
C0086565 (UMLS CUI [1])
C0232804 (UMLS CUI [2])
C0231199 (UMLS CUI [3,1])
C0009429 (UMLS CUI [3,2])
C0232804 (UMLS CUI [2])
C0231199 (UMLS CUI [3,1])
C0009429 (UMLS CUI [3,2])
Radiotherapy to thorax
Item
received thoracic rt before
boolean
C4038705 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnant or breast-feeding women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Communicable Disease
Item
present with active infection
boolean
C0009450 (UMLS CUI [1])
Diabetic - poor control
Item
uncontrolled diabetes
boolean
C0421258 (UMLS CUI [1])
Antineoplastic Agents
Item
concurrent use of other anti-cancer agents
boolean
C0003392 (UMLS CUI [1])