ID

20212

Beskrivning

Study to Evaluate Progression Free Survival in Cancer Patients With Advanced Colorectal Carcinoma With AMT2003; ODM derived from: https://clinicaltrials.gov/show/NCT00405561

Länk

https://clinicaltrials.gov/show/NCT00405561

Nyckelord

Versioner (1)
  1. 2017-02-13 2017-02-13 -
Uppladdad den

13 februari 2017

DOI

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Licens

Creative Commons BY 4.0
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Eligibility Colorectal Carcinoma NCT00405561

Engelsk

Eligibility Colorectal Carcinoma NCT00405561

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
cancer confirmed by histology or cytology
Beskrivning

Malignant Neoplasms

Datatyp

boolean

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

Measurable Disease Quantity

Datatyp

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
Beskrivning

Advanced disease Unresponsive to Treatment | Advanced disease Standard therapy Lacking

Datatyp

boolean

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

Life Expectancy

Datatyp

boolean

Alias
UMLS CUI [1]
C0023671
Exclusion Criteria
Beskrivning

Exclusion Criteria

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

Secondary Neoplasm | CNS metastases | leukemia | Chronic leukemia | Lymphoma | chronic lymphoma | Multiple Myeloma | Multiple Myeloma chronic

Datatyp

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]
C2063391
UMLS CUI [7]
C0026764
UMLS CUI [8,1]
C0026764
UMLS CUI [8,2]
C0205191
body weight below 45 kg
Beskrivning

Body Weight

Datatyp

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
Beskrivning

Pregnancy | Breast Feeding | Females & males of reproductive potential Contraceptive methods Lacking

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3,1]
C4034483
UMLS CUI [3,2]
C0700589
UMLS CUI [3,3]
C0332268
confirmed diagnosis of hiv
Beskrivning

HIV Infection

Datatyp

boolean

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

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

Datatyp

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
Beskrivning

Chemotherapy | Therapeutic radiology procedure

Datatyp

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)
Beskrivning

Operative Surgical Procedures | Effect of surgery Recovering Unsuccessful

Datatyp

boolean

Alias
UMLS CUI [1]
C0543467
UMLS CUI [2,1]
C0544721
UMLS CUI [2,2]
C0521108
UMLS CUI [2,3]
C1272705
participation in a clinical trial less than 30 days prior to entry in the study
Beskrivning

Study Subject Participation Status

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568
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Similar models

Eligibility Colorectal Carcinoma NCT00405561

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Malignant Neoplasms
Item
cancer confirmed by histology or cytology
boolean
C0006826 (UMLS CUI [1])
Measurable Disease Quantity
Item
at least one measurable lesion
boolean
C1513041 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
Advanced disease Unresponsive to Treatment | Advanced disease Standard therapy Lacking
Item
advanced disease refractory to standard therapy or for which no standard therapy exists
boolean
C0679246 (UMLS CUI [1,1])
C0205269 (UMLS CUI [1,2])
C0679246 (UMLS CUI [2,1])
C2936643 (UMLS CUI [2,2])
C0332268 (UMLS CUI [2,3])
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 | chronic lymphoma | Multiple Myeloma | Multiple Myeloma chronic
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])
C2063391 (UMLS CUI [6])
C0026764 (UMLS CUI [7])
C0026764 (UMLS CUI [8,1])
C0205191 (UMLS CUI [8,2])
Body Weight
Item
body weight below 45 kg
boolean
C0005910 (UMLS CUI [1])
Pregnancy | Breast Feeding | Females & males of reproductive potential Contraceptive methods Lacking
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])
C0700589 (UMLS CUI [3,2])
C0332268 (UMLS CUI [3,3])
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 Recovering Unsuccessful
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])
C0521108 (UMLS CUI [2,2])
C1272705 (UMLS CUI [2,3])
Study Subject Participation Status
Item
participation in a clinical trial less than 30 days prior to entry in the study
boolean
C2348568 (UMLS CUI [1])
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