Informations:
Erreur:
ID
16305
Description
T-Cell Response in Patients Receiving Trastuzumab and/or Chemotherapy for HER2-Positive Solid Tumors; ODM derived from: https://clinicaltrials.gov/show/NCT00433407
Lien
https://clinicaltrials.gov/show/NCT00433407
Mots-clés
Versions (1)
- 10/07/2016 10/07/2016 -
Téléchargé le
10 juillet 2016
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 Breast Cancer NCT00433407
Eligibility Breast Cancer NCT00433407
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00433407
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Solid epithelial tumor
Item
diagnosis of solid epithelial tumor, including, but not limited to, the following:
boolean
C0280100 (UMLS CUI [1,1])
C1368683 (UMLS CUI [1,2])
C1368683 (UMLS CUI [1,2])
Breast cancer
Item
breast cancer
boolean
C0678222 (UMLS CUI [1])
Ovarian cancer
Item
ovarian cancer
boolean
C0029925 (UMLS CUI [1])
Lung cancer
Item
lung cancer
boolean
C0242379 (UMLS CUI [1])
Uterine cancer
Item
uterine cancer
boolean
C0153567 (UMLS CUI [1])
Prostate cancer
Item
prostate cancer
boolean
C0600139 (UMLS CUI [1])
her2/neu status by immunohistochemistry or fluorescent in situ hybridization
Item
her2/neu-positive disease by immunohistochemistry or fluorescent in situ hybridization
boolean
C0242957 (UMLS CUI [1,1])
C0021044 (UMLS CUI [1,2])
C0162789 (UMLS CUI [1,3])
C0021044 (UMLS CUI [1,2])
C0162789 (UMLS CUI [1,3])
trastuzumab and/or chemotherapy
Item
must be receiving trastuzumab (herceptin®) and/or chemotherapy (e.g., paclitaxel, docetaxel, fluorouracil, or estramustine)
boolean
C0728747 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
C0392920 (UMLS CUI [2])
Patient characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Absolute Neutrophil Count
Item
absolute neutrophil count > 1,000/mm^3
boolean
C0948762 (UMLS CUI [1])
Absolute Lymphocyte Count
Item
absolute lymphocyte count > 400/mm^3
boolean
C3544087 (UMLS CUI [1])
Platelet Count
Item
platelet count > 90,000/mm^3
boolean
C0032181 (UMLS CUI [1])
Hemoglobin
Item
hemoglobin > 8 g/dl
boolean
C0518015 (UMLS CUI [1])
concurrent therapy
Item
prior concurrent therapy:
boolean
C0009429 (UMLS CUI [1])
Chemotherapy
Item
no other chemotherapy within the past 4 weeks
boolean
C0392920 (UMLS CUI [1])