Information:
Fel:
ID
29747
Beskrivning
Study to Evaluate Tumour Response in Cancer Patients With Advanced Hepatocellular Carcinoma (Liver Cancer) With AMT2003; ODM derived from: https://clinicaltrials.gov/show/NCT00405873
Länk
https://clinicaltrials.gov/show/NCT00405873
Nyckelord
Versioner (1)
- 2018-04-18 2018-04-18 -
Rättsinnehavare
See clinicaltrials.gov
Uppladdad den
18 april 2018
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Hepatocellular Carcinoma NCT00405873
Eligibility Hepatocellular Carcinoma NCT00405873
- StudyEvent: Eligibility
Similar models
Eligibility Hepatocellular Carcinoma NCT00405873
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
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])
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])
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])
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])
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])
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])
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])
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])
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])