ID

31805

Descripción

VEGF Imaging in Renal Cell Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT00831857

Link

https://clinicaltrials.gov/show/NCT00831857

Palabras clave

  1. 29/9/18 29/9/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

29 de septiembre de 2018

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Renal Cell Carcinoma NCT00831857

Eligibility Renal Cell Carcinoma NCT00831857

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
locally advanced irresectable or metastatic renal cell cancer
Descripción

Renal Cell Carcinoma Advanced Locally unresectable | Metastatic Renal Cell Cancer

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0007134
UMLS CUI [1,2]
C0205179
UMLS CUI [1,3]
C1517927
UMLS CUI [1,4]
C1519810
UMLS CUI [2]
C0278678
no untreated brain metastases (ct or mri not necessary in the absence of symptoms)
Descripción

Metastatic malignant neoplasm to brain Untreated Absent | Symptoms Absent | CT Redundant | MRI Redundant

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0220650
UMLS CUI [1,2]
C0332155
UMLS CUI [1,3]
C0332197
UMLS CUI [2,1]
C1457887
UMLS CUI [2,2]
C0332197
UMLS CUI [3,1]
C0040405
UMLS CUI [3,2]
C1313915
UMLS CUI [4,1]
C0024485
UMLS CUI [4,2]
C1313915
no uncontrolled hypertension
Descripción

Uncontrolled hypertension Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1868885
UMLS CUI [1,2]
C0332197
no clinically significant cardiovascular events or disease during the last 12 months
Descripción

Cardiovascular event Absent | Cardiovascular Disease Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1320716
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0007222
UMLS CUI [2,2]
C0332197
no surgery in the last 4 weeks
Descripción

Operative Surgical Procedures Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0543467
UMLS CUI [1,2]
C0332197
no treatment with bevacizumab or another monoclonal antibody with anti-angiogenic properties in the last 4 months
Descripción

Bevacizumab Absent | Monoclonal Antibodies Absent | Angiogenesis Inhibitors Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0796392
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0003250
UMLS CUI [2,2]
C0332197
UMLS CUI [3,1]
C0596087
UMLS CUI [3,2]
C0332197
no treatment with a tyrosine kinase inhibitor during the last 4 weeks
Descripción

Tyrosine kinase inhibitor Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1268567
UMLS CUI [1,2]
C0332197
measurable disease with x-ray or ct scan, at least one site of disease must be unidimensionally measurable as follows: x-ray > 20 mm, spiral ct scan > 10 mm, non-spiral ct scan > 20 mm
Descripción

Measurable Disease X-Ray | Measurable Disease CT scan | Site Measurable Linear X-Ray | Site Measurable Linear Spiral CT scan | Site Measurable Linear CT scan

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1513041
UMLS CUI [1,2]
C0034571
UMLS CUI [2,1]
C1513041
UMLS CUI [2,2]
C0040405
UMLS CUI [3,1]
C1515974
UMLS CUI [3,2]
C1513040
UMLS CUI [3,3]
C0205132
UMLS CUI [3,4]
C0034571
UMLS CUI [4,1]
C1515974
UMLS CUI [4,2]
C1513040
UMLS CUI [4,3]
C0205132
UMLS CUI [4,4]
C0860888
UMLS CUI [5,1]
C1515974
UMLS CUI [5,2]
C1513040
UMLS CUI [5,3]
C0205132
UMLS CUI [5,4]
C0040405
clear cell histology component
Descripción

Clear cell renal cell carcinoma Component

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0279702
UMLS CUI [1,2]
C1705248
not pregnant or nursing
Descripción

Pregnancy Absent | Breast Feeding Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0006147
UMLS CUI [2,2]
C0332197
women of childbearing potential must use effective contraception
Descripción

Childbearing Potential Contraceptive methods

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0700589
absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial
Descripción

Exclusion Criteria | Mental condition Interferes with Protocol Compliance | Condition Familial Interferes with Protocol Compliance | Sociological Factors Interfere with Protocol Compliance | Geographic Factors Interfere with Protocol Compliance

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0680251
UMLS CUI [2,1]
C3840291
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C0525058
UMLS CUI [3,1]
C0348080
UMLS CUI [3,2]
C0241888
UMLS CUI [3,3]
C0521102
UMLS CUI [3,4]
C0525058
UMLS CUI [4,1]
C3850138
UMLS CUI [4,2]
C0521102
UMLS CUI [4,3]
C0525058
UMLS CUI [5,1]
C0017444
UMLS CUI [5,2]
C0521102
UMLS CUI [5,3]
C0525058
before patient randomization, written informed consent must be given according to gcp, and local regulations
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430

Similar models

Eligibility Renal Cell Carcinoma NCT00831857

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Renal Cell Carcinoma Advanced Locally unresectable | Metastatic Renal Cell Cancer
Item
locally advanced irresectable or metastatic renal cell cancer
boolean
C0007134 (UMLS CUI [1,1])
C0205179 (UMLS CUI [1,2])
C1517927 (UMLS CUI [1,3])
C1519810 (UMLS CUI [1,4])
C0278678 (UMLS CUI [2])
Metastatic malignant neoplasm to brain Untreated Absent | Symptoms Absent | CT Redundant | MRI Redundant
Item
no untreated brain metastases (ct or mri not necessary in the absence of symptoms)
boolean
C0220650 (UMLS CUI [1,1])
C0332155 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C1457887 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0040405 (UMLS CUI [3,1])
C1313915 (UMLS CUI [3,2])
C0024485 (UMLS CUI [4,1])
C1313915 (UMLS CUI [4,2])
Uncontrolled hypertension Absent
Item
no uncontrolled hypertension
boolean
C1868885 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Cardiovascular event Absent | Cardiovascular Disease Absent
Item
no clinically significant cardiovascular events or disease during the last 12 months
boolean
C1320716 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0007222 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Operative Surgical Procedures Absent
Item
no surgery in the last 4 weeks
boolean
C0543467 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Bevacizumab Absent | Monoclonal Antibodies Absent | Angiogenesis Inhibitors Absent
Item
no treatment with bevacizumab or another monoclonal antibody with anti-angiogenic properties in the last 4 months
boolean
C0796392 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0003250 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0596087 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
Tyrosine kinase inhibitor Absent
Item
no treatment with a tyrosine kinase inhibitor during the last 4 weeks
boolean
C1268567 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Measurable Disease X-Ray | Measurable Disease CT scan | Site Measurable Linear X-Ray | Site Measurable Linear Spiral CT scan | Site Measurable Linear CT scan
Item
measurable disease with x-ray or ct scan, at least one site of disease must be unidimensionally measurable as follows: x-ray > 20 mm, spiral ct scan > 10 mm, non-spiral ct scan > 20 mm
boolean
C1513041 (UMLS CUI [1,1])
C0034571 (UMLS CUI [1,2])
C1513041 (UMLS CUI [2,1])
C0040405 (UMLS CUI [2,2])
C1515974 (UMLS CUI [3,1])
C1513040 (UMLS CUI [3,2])
C0205132 (UMLS CUI [3,3])
C0034571 (UMLS CUI [3,4])
C1515974 (UMLS CUI [4,1])
C1513040 (UMLS CUI [4,2])
C0205132 (UMLS CUI [4,3])
C0860888 (UMLS CUI [4,4])
C1515974 (UMLS CUI [5,1])
C1513040 (UMLS CUI [5,2])
C0205132 (UMLS CUI [5,3])
C0040405 (UMLS CUI [5,4])
Clear cell renal cell carcinoma Component
Item
clear cell histology component
boolean
C0279702 (UMLS CUI [1,1])
C1705248 (UMLS CUI [1,2])
Pregnancy Absent | Breast Feeding Absent
Item
not pregnant or nursing
boolean
C0032961 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0006147 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Childbearing Potential Contraceptive methods
Item
women of childbearing potential must use effective contraception
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
Exclusion Criteria | Mental condition Interferes with Protocol Compliance | Condition Familial Interferes with Protocol Compliance | Sociological Factors Interfere with Protocol Compliance | Geographic Factors Interfere with Protocol Compliance
Item
absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial
boolean
C0680251 (UMLS CUI [1])
C3840291 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0525058 (UMLS CUI [2,3])
C0348080 (UMLS CUI [3,1])
C0241888 (UMLS CUI [3,2])
C0521102 (UMLS CUI [3,3])
C0525058 (UMLS CUI [3,4])
C3850138 (UMLS CUI [4,1])
C0521102 (UMLS CUI [4,2])
C0525058 (UMLS CUI [4,3])
C0017444 (UMLS CUI [5,1])
C0521102 (UMLS CUI [5,2])
C0525058 (UMLS CUI [5,3])
Informed Consent
Item
before patient randomization, written informed consent must be given according to gcp, and local regulations
boolean
C0021430 (UMLS CUI [1])

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