ID

44503

Descripción

Phase I/II Study of OPB-31121 in Patients With Progressive Hepatocellular Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT01406574

Link

https://clinicaltrials.gov/show/NCT01406574

Palabras clave

Versiones (2)
  1. 19/2/20 19/2/20 -
  2. 27/9/21 27/9/21 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

27 de septiembre de 2021

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Hepatocellular Carcinoma NCT01406574

Inglés

Eligibility Hepatocellular Carcinoma NCT01406574

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with histopathologically or clinically confirmed diagnosis of hepatocellular carcinoma
Descripción

Liver carcinoma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2239176
patients with child-pugh classification a or b
Descripción

Child-Pugh Classification

Tipo de datos

boolean

Alias
UMLS CUI [1]
C4050412
patients unresponsive to standard therapy or for whom standard therapy is intolerable, or for whom there is no appropriate therapy
Descripción

Unresponsive to Standard therapy | Intolerance Standard therapy | Therapy Appropriate Unavailable

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0205269
UMLS CUI [1,2]
C2936643
UMLS CUI [2,1]
C0231199
UMLS CUI [2,2]
C2936643
UMLS CUI [3,1]
C0087111
UMLS CUI [3,2]
C1548787
UMLS CUI [3,3]
C0686905
patients who are able to take oral medication
Descripción

Able to swallow Oral medication

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2712086
UMLS CUI [1,2]
C0175795
patients age 20 to 79 years (inclusive) at time of informed consent
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
patients with an ecog performance status score of 0-2
Descripción

ECOG performance status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1520224
patients have the eligible organ function.
Descripción

Organ function

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0678852
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with a primary malignant tumor
Descripción

Primary malignant neoplasm

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1306459
patients with a history of liver transplant
Descripción

Transplantation of liver

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023911
patients with brain metastases
Descripción

Metastatic malignant neoplasm to brain

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0220650
patients with a complication of uncontrolled
Descripción

Complication

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0009566
patients with a psychiatric disorder that might cause difficulty in obtaining informed consent or in conducting the trial
Descripción

Mental disorder Difficulty with Informed Consent | Mental disorder Difficulty with Completion of clinical trial

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0004936
UMLS CUI [1,2]
C0332218
UMLS CUI [1,3]
C0021430
UMLS CUI [2,1]
C0004936
UMLS CUI [2,2]
C0332218
UMLS CUI [2,3]
C2732579
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Similar models

Eligibility Hepatocellular Carcinoma NCT01406574

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Liver carcinoma
Item
patients with histopathologically or clinically confirmed diagnosis of hepatocellular carcinoma
boolean
C2239176 (UMLS CUI [1])
Child-Pugh Classification
Item
patients with child-pugh classification a or b
boolean
C4050412 (UMLS CUI [1])
Unresponsive to Standard therapy | Intolerance Standard therapy | Therapy Appropriate Unavailable
Item
patients unresponsive to standard therapy or for whom standard therapy is intolerable, or for whom there is no appropriate therapy
boolean
C0205269 (UMLS CUI [1,1])
C2936643 (UMLS CUI [1,2])
C0231199 (UMLS CUI [2,1])
C2936643 (UMLS CUI [2,2])
C0087111 (UMLS CUI [3,1])
C1548787 (UMLS CUI [3,2])
C0686905 (UMLS CUI [3,3])
Able to swallow Oral medication
Item
patients who are able to take oral medication
boolean
C2712086 (UMLS CUI [1,1])
C0175795 (UMLS CUI [1,2])
Age
Item
patients age 20 to 79 years (inclusive) at time of informed consent
boolean
C0001779 (UMLS CUI [1])
ECOG performance status
Item
patients with an ecog performance status score of 0-2
boolean
C1520224 (UMLS CUI [1])
Organ function
Item
patients have the eligible organ function.
boolean
C0678852 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Primary malignant neoplasm
Item
patients with a primary malignant tumor
boolean
C1306459 (UMLS CUI [1])
Transplantation of liver
Item
patients with a history of liver transplant
boolean
C0023911 (UMLS CUI [1])
Metastatic malignant neoplasm to brain
Item
patients with brain metastases
boolean
C0220650 (UMLS CUI [1])
Complication
Item
patients with a complication of uncontrolled
boolean
C0009566 (UMLS CUI [1])
Mental disorder Difficulty with Informed Consent | Mental disorder Difficulty with Completion of clinical trial
Item
patients with a psychiatric disorder that might cause difficulty in obtaining informed consent or in conducting the trial
boolean
C0004936 (UMLS CUI [1,1])
C0332218 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,3])
C0004936 (UMLS CUI [2,1])
C0332218 (UMLS CUI [2,2])
C2732579 (UMLS CUI [2,3])
Volver a la parte superior de la página 

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