ID

29747

Beschrijving

Study to Evaluate Tumour Response in Cancer Patients With Advanced Hepatocellular Carcinoma (Liver Cancer) With AMT2003; ODM derived from: https://clinicaltrials.gov/show/NCT00405873

Link

https://clinicaltrials.gov/show/NCT00405873

Trefwoorden

Versies (1)
  1. 18-04-18 18-04-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

18 april 2018

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Hepatocellular Carcinoma NCT00405873

Engels

Eligibility Hepatocellular Carcinoma NCT00405873

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
cancer confirmed by histology or cytology
Beschrijving

Malignant Neoplasms

Datatype

boolean

Alias
UMLS CUI [1]
C0006826
at least one measurable lesion
Beschrijving

Measurable Lesion Quantity

Datatype

boolean

Alias
UMLS CUI [1,1]
C1513041
UMLS CUI [1,2]
C1265611
advanced disease refractory to standard therapy or for which no standard therapy exists
Beschrijving

Advanced disease | Standard of Care Unresponsive to Treatment | Standard therapy Lacking

Datatype

boolean

Alias
UMLS CUI [1]
C0679246
UMLS CUI [2,1]
C2936643
UMLS CUI [2,2]
C0205269
UMLS CUI [3,1]
C2936643
UMLS CUI [3,2]
C0332268
life expectancy of at least 3 months
Beschrijving

Life Expectancy

Datatype

boolean

Alias
UMLS CUI [1]
C0023671
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
known secondary neoplasia or central nervous system (cns) metastases; acute or chronic leukemia, lymphoma or multiple myeloma
Beschrijving

Secondary Neoplasm | CNS metastases | Leukemia | Chronic leukemia | Lymphoma | Multiple Myeloma

Datatype

boolean

Alias
UMLS CUI [1]
C2939419
UMLS CUI [2]
C0686377
UMLS CUI [3]
C0023418
UMLS CUI [4]
C1279296
UMLS CUI [5]
C0024299
UMLS CUI [6]
C0026764
body weight below 45 kg
Beschrijving

Body Weight

Datatype

boolean

Alias
UMLS CUI [1]
C0005910
female patients who are pregnant or breast feeding or adults of reproductive potential not employing effective method of birth control
Beschrijving

Pregnancy | Breast Feeding | Reproductive potential Adult Contraceptive methods Absent

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3,1]
C4034483
UMLS CUI [3,2]
C0001675
UMLS CUI [3,3]
C0700589
UMLS CUI [3,4]
C0332197
confirmed diagnosis of hiv
Beschrijving

HIV Infection

Datatype

boolean

Alias
UMLS CUI [1]
C0019693
insulin dependent diabetes mellitus / abnormal glucose tolerance test (gtt) / latent diabetes mellitus type i or ii
Beschrijving

Diabetes Mellitus, Insulin-Dependent | Abnormal glucose tolerance test | Insulin-Dependent Diabetes Mellitus Latent | Non-Insulin-Dependent Diabetes Mellitus Latent

Datatype

boolean

Alias
UMLS CUI [1]
C0011854
UMLS CUI [2]
C0159069
UMLS CUI [3,1]
C0011854
UMLS CUI [3,2]
C0205275
UMLS CUI [4,1]
C0011860
UMLS CUI [4,2]
C0205275
chemotherapy or radiotherapy less than 4 weeks prior to entry
Beschrijving

Chemotherapy | Therapeutic radiology procedure

Datatype

boolean

Alias
UMLS CUI [1]
C0392920
UMLS CUI [2]
C1522449
surgery less than 2 weeks prior to entry (or not recovered from effects of surgery)
Beschrijving

Operative Surgical Procedures | Effect of surgery Recovery Lacking

Datatype

boolean

Alias
UMLS CUI [1]
C0543467
UMLS CUI [2,1]
C0544721
UMLS CUI [2,2]
C2004454
UMLS CUI [2,3]
C0332268
participation in a clinical trial less than 30 days prior to entry into study
Beschrijving

Study Subject Participation Status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
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Similar models

Eligibility Hepatocellular Carcinoma NCT00405873

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Malignant Neoplasms
Item
cancer confirmed by histology or cytology
boolean
C0006826 (UMLS CUI [1])
Measurable Lesion Quantity
Item
at least one measurable lesion
boolean
C1513041 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
Advanced disease | Standard of Care Unresponsive to Treatment | Standard therapy Lacking
Item
advanced disease refractory to standard therapy or for which no standard therapy exists
boolean
C0679246 (UMLS CUI [1])
C2936643 (UMLS CUI [2,1])
C0205269 (UMLS CUI [2,2])
C2936643 (UMLS CUI [3,1])
C0332268 (UMLS CUI [3,2])
Life Expectancy
Item
life expectancy of at least 3 months
boolean
C0023671 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Secondary Neoplasm | CNS metastases | Leukemia | Chronic leukemia | Lymphoma | Multiple Myeloma
Item
known secondary neoplasia or central nervous system (cns) metastases; acute or chronic leukemia, lymphoma or multiple myeloma
boolean
C2939419 (UMLS CUI [1])
C0686377 (UMLS CUI [2])
C0023418 (UMLS CUI [3])
C1279296 (UMLS CUI [4])
C0024299 (UMLS CUI [5])
C0026764 (UMLS CUI [6])
Body Weight
Item
body weight below 45 kg
boolean
C0005910 (UMLS CUI [1])
Pregnancy | Breast Feeding | Reproductive potential Adult Contraceptive methods Absent
Item
female patients who are pregnant or breast feeding or adults of reproductive potential not employing effective method of birth control
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C4034483 (UMLS CUI [3,1])
C0001675 (UMLS CUI [3,2])
C0700589 (UMLS CUI [3,3])
C0332197 (UMLS CUI [3,4])
HIV Infection
Item
confirmed diagnosis of hiv
boolean
C0019693 (UMLS CUI [1])
Diabetes Mellitus, Insulin-Dependent | Abnormal glucose tolerance test | Insulin-Dependent Diabetes Mellitus Latent | Non-Insulin-Dependent Diabetes Mellitus Latent
Item
insulin dependent diabetes mellitus / abnormal glucose tolerance test (gtt) / latent diabetes mellitus type i or ii
boolean
C0011854 (UMLS CUI [1])
C0159069 (UMLS CUI [2])
C0011854 (UMLS CUI [3,1])
C0205275 (UMLS CUI [3,2])
C0011860 (UMLS CUI [4,1])
C0205275 (UMLS CUI [4,2])
Chemotherapy | Therapeutic radiology procedure
Item
chemotherapy or radiotherapy less than 4 weeks prior to entry
boolean
C0392920 (UMLS CUI [1])
C1522449 (UMLS CUI [2])
Operative Surgical Procedures | Effect of surgery Recovery Lacking
Item
surgery less than 2 weeks prior to entry (or not recovered from effects of surgery)
boolean
C0543467 (UMLS CUI [1])
C0544721 (UMLS CUI [2,1])
C2004454 (UMLS CUI [2,2])
C0332268 (UMLS CUI [2,3])
Study Subject Participation Status
Item
participation in a clinical trial less than 30 days prior to entry into study
boolean
C2348568 (UMLS CUI [1])
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