ID

44503

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT01406574

Nyckelord

  1. 2020-02-19 2020-02-19 -
  2. 2021-09-27 2021-09-27 -
Rättsinnehavare

See clinicaltrials.gov

Uppladdad den

27 september 2021

DOI

För en begäran logga in.

Licens

Creative Commons BY 4.0

Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Itemgroup-kommentar för :

Item-kommentar för :

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

Eligibility Hepatocellular Carcinoma NCT01406574

Eligibility Hepatocellular Carcinoma NCT01406574

Inclusion Criteria
Beskrivning

Inclusion Criteria

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

Liver carcinoma

Datatyp

boolean

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

Child-Pugh Classification

Datatyp

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
Beskrivning

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

Datatyp

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
Beskrivning

Able to swallow Oral medication

Datatyp

boolean

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

Age

Datatyp

boolean

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

ECOG performance status

Datatyp

boolean

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

Organ function

Datatyp

boolean

Alias
UMLS CUI [1]
C0678852
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with a primary malignant tumor
Beskrivning

Primary malignant neoplasm

Datatyp

boolean

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

Transplantation of liver

Datatyp

boolean

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

Metastatic malignant neoplasm to brain

Datatyp

boolean

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

Complication

Datatyp

boolean

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

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

Datatyp

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

Similar models

Eligibility Hepatocellular Carcinoma NCT01406574

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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])

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial