ID

20622

Beschrijving

Preliminary Results for the Double-dose Adenovirus-mediated Adjuvant Therapy Improving Outcome of Liver Transplantation in Patients With Advanced Hepatocellular Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT02202564

Link

https://clinicaltrials.gov/show/NCT02202564

Trefwoorden

  1. 07-03-17 07-03-17 -
Geüploaded op

7 maart 2017

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Liver Cancer NCT02202564

Eligibility Liver Cancer NCT02202564

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
18~70 years of age (male and female).
Beschrijving

age, gender

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C0079399
clinical diagnosis of advanced hepatocellular carcinoma who could accept liver transplantation
Beschrijving

hepatocellular carcinoma, liver transplantation

Datatype

boolean

Alias
UMLS CUI [1]
C0278774
UMLS CUI [2]
C0023911
patients who had unresectable hcc >5 cm and no metastasis in lungs and bones were eligible to participate in this study. tumor involvement in the intrahepatic and extrahepatic portal branches was not considered to be an exclusion criterion.
Beschrijving

localized unresectable adult primary liver cancer | Secondary malignant neoplasm of lung | Secondary malignant neoplasm of bone | Tumor extent of invasion; Structure of branch of portal vein

Datatype

boolean

Alias
UMLS CUI [1]
C0278773
UMLS CUI [2]
C0475440
UMLS CUI [3]
C0153676
UMLS CUI [4]
C0153690
UMLS CUI [5,1]
C1269793
UMLS CUI [5,2]
C0226736
no prior chemotherapy, radiation therapy, targeted therapy or other kind of biological treatment within 4 weeks.
Beschrijving

Prior Chemotherapy | prior radiation therapy | Prior Therapy; Targeted cancer therapy | Prior Therapy; Biological Response Modifier Therapy

Datatype

boolean

Alias
UMLS CUI [1]
C1514457
UMLS CUI [2]
C0279134
UMLS CUI [3,1]
C1514463
UMLS CUI [3,2]
C3854476
UMLS CUI [4,1]
C1514463
UMLS CUI [4,2]
C0005527
provide written informed consent
Beschrijving

informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
metastasis in lungs and bones
Beschrijving

metastasis in lungs and bones

Datatype

boolean

Alias
UMLS CUI [1]
C0153676
UMLS CUI [2]
C0153690
invasion in main vescular.
Beschrijving

invasion in main vescular

Datatype

boolean

Alias
UMLS CUI [1]
C0521157
contraindications of liver transplantation
Beschrijving

contraindications of liver transplantation

Datatype

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0023911
contraindications of operation of other organ system
Beschrijving

contraindications of operation of other organ system

Datatype

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0543467
hypersensitivity to adenovirus, gcv or similar drugs
Beschrijving

hypersensitivity to adenovirus or gcv

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0001483
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0017066
accept clinical trials of other drugs
Beschrijving

accept clinical trials of other drugs

Datatype

boolean

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C0013227
immunological deficit
Beschrijving

immunological deficit

Datatype

boolean

Alias
UMLS CUI [1]
C0021053
active pregnancy
Beschrijving

pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
unable or unwilling to sign informed consents
Beschrijving

informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430

Similar models

Eligibility Liver Cancer NCT02202564

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
age, gender
Item
18~70 years of age (male and female).
boolean
C0001779 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
hepatocellular carcinoma, liver transplantation
Item
clinical diagnosis of advanced hepatocellular carcinoma who could accept liver transplantation
boolean
C0278774 (UMLS CUI [1])
C0023911 (UMLS CUI [2])
localized unresectable adult primary liver cancer | Secondary malignant neoplasm of lung | Secondary malignant neoplasm of bone | Tumor extent of invasion; Structure of branch of portal vein
Item
patients who had unresectable hcc >5 cm and no metastasis in lungs and bones were eligible to participate in this study. tumor involvement in the intrahepatic and extrahepatic portal branches was not considered to be an exclusion criterion.
boolean
C0278773 (UMLS CUI [1])
C0475440 (UMLS CUI [2])
C0153676 (UMLS CUI [3])
C0153690 (UMLS CUI [4])
C1269793 (UMLS CUI [5,1])
C0226736 (UMLS CUI [5,2])
Prior Chemotherapy | prior radiation therapy | Prior Therapy; Targeted cancer therapy | Prior Therapy; Biological Response Modifier Therapy
Item
no prior chemotherapy, radiation therapy, targeted therapy or other kind of biological treatment within 4 weeks.
boolean
C1514457 (UMLS CUI [1])
C0279134 (UMLS CUI [2])
C1514463 (UMLS CUI [3,1])
C3854476 (UMLS CUI [3,2])
C1514463 (UMLS CUI [4,1])
C0005527 (UMLS CUI [4,2])
informed consent
Item
provide written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
metastasis in lungs and bones
Item
metastasis in lungs and bones
boolean
C0153676 (UMLS CUI [1])
C0153690 (UMLS CUI [2])
invasion in main vescular
Item
invasion in main vescular.
boolean
C0521157 (UMLS CUI [1])
contraindications of liver transplantation
Item
contraindications of liver transplantation
boolean
C1301624 (UMLS CUI [1,1])
C0023911 (UMLS CUI [1,2])
contraindications of operation of other organ system
Item
contraindications of operation of other organ system
boolean
C1301624 (UMLS CUI [1,1])
C0543467 (UMLS CUI [1,2])
hypersensitivity to adenovirus or gcv
Item
hypersensitivity to adenovirus, gcv or similar drugs
boolean
C0020517 (UMLS CUI [1,1])
C0001483 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0017066 (UMLS CUI [2,2])
accept clinical trials of other drugs
Item
accept clinical trials of other drugs
boolean
C0008976 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
immunological deficit
Item
immunological deficit
boolean
C0021053 (UMLS CUI [1])
pregnancy
Item
active pregnancy
boolean
C0032961 (UMLS CUI [1])
informed consent
Item
unable or unwilling to sign informed consents
boolean
C0021430 (UMLS CUI [1])

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