Informations:
Erreur:
ID
22340
Description
Pilot Study of Imatinib (Gleevec) as Treatment for Advanced Thymic Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT00314873
Lien
https://clinicaltrials.gov/show/NCT00314873
Mots-clés
Versions (1)
- 30/05/2017 30/05/2017 -
Téléchargé le
30 mai 2017
DOI
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Licence
Creative Commons BY 4.0
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Eligibility Thymic Carcinoma NCT00314873
Eligibility Thymic Carcinoma NCT00314873
- StudyEvent: Eligibility
Similar models
Eligibility Thymic Carcinoma NCT00314873
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
c-kit and pdgfr positive thymic carcinoma
Item
histological or cytological proof of advanced c-kit positive or pdgfr positive thymic carcinoma. for protocol purposes, advanced disease is defined as disease
boolean
C0205969 (UMLS CUI [1,1])
C0072470 (UMLS CUI [1,2])
C0071253 (UMLS CUI [1,3])
C0072470 (UMLS CUI [1,2])
C0071253 (UMLS CUI [1,3])
measuable thymic carcinoma lesion
Item
patient must have at least one documented measurable lesion obtained by imaging within 28 days prior to being registered for protocol therapy.
boolean
C0205969 (UMLS CUI [1,1])
C1513041 (UMLS CUI [1,2])
C1513041 (UMLS CUI [1,2])
imatinib
Item
no prior imatinib therapy.
boolean
C0935989 (UMLS CUI [1])
age
Item
age > 18 years at the time of consent
boolean
C0001779 (UMLS CUI [1])
ecog
Item
ecog performance status of 0 or 1
boolean
C1520224 (UMLS CUI [1])
anc, platelet count, total bilirubin, serum creatinine, alt, ast
Item
anc ≥ 1500/mm3,platelet count ≥ 100,000/mm,total bilirubin < 1.5uln,3.10 serum creatinine ≤ 1.7 mg/dl,alt and ast ≤ 3 x uln
boolean
C0948762 (UMLS CUI [1])
C0005821 (UMLS CUI [2])
C0201913 (UMLS CUI [3])
C0201976 (UMLS CUI [4])
C0201836 (UMLS CUI [5])
C0201899 (UMLS CUI [6])
C0005821 (UMLS CUI [2])
C0201913 (UMLS CUI [3])
C0201976 (UMLS CUI [4])
C0201836 (UMLS CUI [5])
C0201899 (UMLS CUI [6])
infections
Item
clinically significant infections as judged by the treating investigator
boolean
C0009450 (UMLS CUI [1])
comorbidity
Item
clinically significant concurrent illnesses
boolean
C0009488 (UMLS CUI [1])
females of childbearing potential birth control, breastfeeding
Item
females of childbearing potential not using birth control or breastfeeding
boolean
C1960468 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0006147 (UMLS CUI [2])
C0700589 (UMLS CUI [1,2])
C0006147 (UMLS CUI [2])
bone marrow radiation therapy
Item
prior radiation therapy > 25% of the bone marrow
boolean
C1522449 (UMLS CUI [1,1])
C0005953 (UMLS CUI [1,2])
C0005953 (UMLS CUI [1,2])
symptomatic brain metastasis
Item
symptomatic brain metastasis
boolean
C0220650 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C0231220 (UMLS CUI [1,2])
cardiac problems
Item
history of grade iii/iv cardiac problems
boolean
C0262402 (UMLS CUI [1])
major surgery
Item
history of major surgery within 14 days prior to being registered
boolean
C0679637 (UMLS CUI [1])
investigational agent
Item
treatment with any investigational agent within 30 days prior to being registered for protocol therapy.
boolean
C0013230 (UMLS CUI [1])