Informations:
Erreur:
ID
12999
Description
Hepatic Arterial Infusion With Floxuridine and Dexamethasone in Combination With Intravenous Oxaliplatin Plus Irinotecan in Patients With Unresectable Hepatic Metastases From Colorectal Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00695201
Lien
https://clinicaltrials.gov/show/NCT00695201
Mots-clés
Versions (1)
- 10/01/2016 10/01/2016 -
Téléchargé le
10 janvier 2016
DOI
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Licence
Creative Commons BY 4.0
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Eligibility Colon Cancer NCT00695201
Eligibility Colon Cancer NCT00695201
- StudyEvent: Eligibility
Similar models
Eligibility Colon Cancer NCT00695201
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
histology
Item
history of histologically confirmed colorectal adenocarcinoma metastatic to the liver with no clinical or radiographic evidence of extrahepatic disease.
boolean
C0019638 (UMLS CUI [1,1])
C1319315 (UMLS CUI [1,2])
C0494165 (UMLS CUI [1,3])
C1319315 (UMLS CUI [1,2])
C0494165 (UMLS CUI [1,3])
diagnosis confirmation
Item
confirmation of diagnosis must be performed at mskcc.
boolean
C0011900 (UMLS CUI [1,1])
C0750484 (UMLS CUI [1,2])
C0750484 (UMLS CUI [1,2])
liver metastases
Item
patient's liver metastases must be deemed unresectable and comprise <70% of the liver parenchyma.
boolean
C0494165 (UMLS CUI [1,1])
C1519810 (UMLS CUI [1,2])
C0736268 (UMLS CUI [2])
C1519810 (UMLS CUI [1,2])
C0736268 (UMLS CUI [2])
chemotherapy
Item
a patient may have had prior chemotherapy or be previously untreated.
boolean
C0392920 (UMLS CUI [1])
floxuridine oxaliplatin
Item
patient may not have received prior treatment with fudr or >2 doses of oxaliplatin.
boolean
C0069717 (UMLS CUI [1])
C0016343 (UMLS CUI [2])
C0016343 (UMLS CUI [2])
kps
Item
kps > or = to 60%.
boolean
C0206065 (UMLS CUI [1])
wbc, platelet count
Item
wbc > or = to 3,000 cells/mm3 and platelet count > or = to 100,000 cells/mm3 within 14 days of registration.
boolean
C0023508 (UMLS CUI [1])
C0032181 (UMLS CUI [2])
C0032181 (UMLS CUI [2])
creatinine
Item
creatinine < or = to 1.5 mg/dl within 14 days of registration.
boolean
C0201976 (UMLS CUI [1])
bilirubin
Item
total serum bilirubin < or = 2.0 mg/dl within 14 days of registration.
boolean
C1278039 (UMLS CUI [1])
malignancies
Item
no active concurrent malignancies: except a patient's potentially resectable colorectal primary.
boolean
C0006826 (UMLS CUI [1])
obstruction
Item
patient must not have obstruction of gi or gu tract.
boolean
C0028778 (UMLS CUI [1,1])
C0042066 (UMLS CUI [1,2])
C0028778 (UMLS CUI [2,1])
C0017189 (UMLS CUI [2,2])
C0042066 (UMLS CUI [1,2])
C0028778 (UMLS CUI [2,1])
C0017189 (UMLS CUI [2,2])
peripheral sensory neuropathy
Item
patient must not have current, symptomatic peripheral sensory neuropathy.
boolean
C0151313 (UMLS CUI [1])
radiotherapy
Item
no prior radiation to liver.
boolean
C0948510 (UMLS CUI [1])
comorbidity
Item
no active infection, ascites, or hepatic encephalopathy.
boolean
C0009488 (UMLS CUI [1])
age
Item
age ≥ 18 years.
boolean
C0001779 (UMLS CUI [1])
pregnancy, lactation
Item
female patients cannot be pregnant or lactating.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
informed consent
Item
signed informed consent.
boolean
C0021430 (UMLS CUI [1])