ID

44503

Description

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

Lien

https://clinicaltrials.gov/show/NCT01406574

Mots-clés

  1. 19/02/2020 19/02/2020 -
  2. 27/09/2021 27/09/2021 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

27 septembre 2021

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Hepatocellular Carcinoma NCT01406574

Eligibility Hepatocellular Carcinoma NCT01406574

Inclusion Criteria
Description

Inclusion Criteria

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

Liver carcinoma

Type de données

boolean

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

Child-Pugh Classification

Type de données

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
Description

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

Type de données

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
Description

Able to swallow Oral medication

Type de données

boolean

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

Age

Type de données

boolean

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

ECOG performance status

Type de données

boolean

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

Organ function

Type de données

boolean

Alias
UMLS CUI [1]
C0678852
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with a primary malignant tumor
Description

Primary malignant neoplasm

Type de données

boolean

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

Transplantation of liver

Type de données

boolean

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

Metastatic malignant neoplasm to brain

Type de données

boolean

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

Complication

Type de données

boolean

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

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

Type de données

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
Type
Description | Question | Decode (Coded Value)
Type de données
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])

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