Informatie:
Fout:
ID
43867
Beschrijving
Synergistic Treatment for Hepatocellular Carcinoma (HCC) Using TACE With Antiangiogenesis; ODM derived from: https://clinicaltrials.gov/show/NCT00518557
Link
https://clinicaltrials.gov/show/NCT00518557
Trefwoorden
Versies (2)
- 27-06-17 27-06-17 -
- 20-09-21 20-09-21 -
Geüploaded op
20 september 2021
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Hepatocellular Carcinoma NCT00518557
Eligibility Hepatocellular Carcinoma NCT00518557
- StudyEvent: Eligibility
Similar models
Eligibility Hepatocellular Carcinoma NCT00518557
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
ID.1
Item
patients with cytologically or histologically documented hcc, who are candidates for tace
boolean
C2239176 (UMLS CUI [1,1])
C3539919 (UMLS CUI [1,2])
C3539919 (UMLS CUI [1,2])
ID.2
Item
child-pugh child a or b
boolean
C4050412 (UMLS CUI [1])
ID.3
Item
age >= 18
boolean
C0001779 (UMLS CUI [1])
ID.4
Item
measurable disease by recist criteria;
boolean
C1709926 (UMLS CUI [1])
ID.5
Item
performance status ecog 0-2
boolean
C1520224 (UMLS CUI [1])
ID.6
Item
previous local therapy completed > 4 weeks
boolean
C1517925 (UMLS CUI [1])
ID.7
Item
written informed consent signed
boolean
C0021430 (UMLS CUI [1])
ID.8
Item
normal organ and marrow function defined as:
boolean
C0678852 (UMLS CUI [1])
ID.10
Item
wbc ≥ 3,000/µl platelet count > 80,000/mm3
boolean
C0018957 (UMLS CUI [1,1])
C0023516 (UMLS CUI [1,2])
C0032181 (UMLS CUI [1,3])
C0023516 (UMLS CUI [1,2])
C0032181 (UMLS CUI [1,3])
ID.11
Item
haemoglobin > 9g/dl
boolean
C0019046 (UMLS CUI [1])
ID.12
Item
hepatic: albumin ≥ 2.8 g/dl. serum total bilirubin ≤ 3 mg/dl; ast or alt < 5 x uln
boolean
C0201838 (UMLS CUI [1,1])
C1278039 (UMLS CUI [1,2])
C0004002 (UMLS CUI [1,3])
C0001899 (UMLS CUI [1,4])
C1278039 (UMLS CUI [1,2])
C0004002 (UMLS CUI [1,3])
C0001899 (UMLS CUI [1,4])
ID.13
Item
renal: creatinine < 1.5 x uln
boolean
C0010294 (UMLS CUI [1])
ID.14
Item
metastases
boolean
C0027627 (UMLS CUI [1])
ID.15
Item
prior or concomitant chemotherapy or radiation therapy
boolean
C3178775 (UMLS CUI [1])
ID.16
Item
vegf/vegfr- inhibitors or other anti-angiogenesis agents
boolean
C1257849 (UMLS CUI [1])
ID.17
Item
severe and/or uncontrolled medical conditions:
boolean
C0012634 (UMLS CUI [1])
ID.18
Item
congestive heart failure, serious cardiac arrhythmia, active coronary artery
boolean
C0018799 (UMLS CUI [1])
ID.19
Item
severe renal impairment
boolean
C0022658 (UMLS CUI [1])
ID.20
Item
patients who anticipate receiving major surgery during the course of the
boolean
C0679637 (UMLS CUI [1])
ID.21
Item
pregnant or breastfeeding patients
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
C0006147 (UMLS CUI [1,2])
ID.22
Item
evidence of bleeding diathesis
boolean
C0005779 (UMLS CUI [1])