ID

28359

Beskrivning

Health Economic Evaluation of Primovist-enhanced Liver MRI; ODM derived from: https://clinicaltrials.gov/show/NCT00764621

Länk

https://clinicaltrials.gov/show/NCT00764621

Nyckelord

Versioner (1)
  1. 2018-01-07 2018-01-07 -
Rättsinnehavare

See clinicaltrials.gov

Uppladdad den

7 januari 2018

DOI

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Licens

Creative Commons BY 4.0
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Eligibility Colorectal Neoplasms NCT00764621

Engelsk

Eligibility Colorectal Neoplasms NCT00764621

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with known or suspected metachronous liver metastases secondary to colorectal cancer who are scheduled for further contrast-enhanced tomographic imaging
Beskrivning

Secondary malignant neoplasm of liver Secondary to Colorectal Carcinoma | Secondary malignant neoplasm of liver Suspected Secondary to Colorectal Carcinoma | Contrast Enhanced CT Scheduled

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0494165
UMLS CUI [1,2]
C0175668
UMLS CUI [1,3]
C0009402
UMLS CUI [2,1]
C0494165
UMLS CUI [2,2]
C0750491
UMLS CUI [2,3]
C0175668
UMLS CUI [2,4]
C0009402
UMLS CUI [3,1]
C1512095
UMLS CUI [3,2]
C0205539
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients (men or women) under 18 years of age
Beskrivning

Age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
patients who have received any contrast material within 24 hours before injection of study drug, or who are scheduled to receive any contrast material within 24 hours after injection
Beskrivning

Contrast Media Received | Contrast Media Scheduled

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0009924
UMLS CUI [1,2]
C1514756
UMLS CUI [2,1]
C0009924
UMLS CUI [2,2]
C0205539
patients not eligible to contrast media (cm) injection according to product labeling
Beskrivning

Ineligibility Contrast Media Injection

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1512714
UMLS CUI [1,2]
C0009924
UMLS CUI [1,3]
C1533685
women who are pregnant, lactating or who are of childbearing potential and have not had a negative urine pregnancy test at baseline visit(s)
Beskrivning

Pregnancy | Breast Feeding | Childbearing Potential Urine pregnancy test negative Lacking

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3,1]
C3831118
UMLS CUI [3,2]
C0430057
UMLS CUI [3,3]
C0332268
patients scheduled for liver-specific mri other than primovist-enhanced mri, i.e. multihance-, teslascan- or spio-enhanced mri
Beskrivning

MRI of Liver Scheduled | Exception MRI Eovist Enhanced | Exception MRI MultiHance Enhanced | Exception MRI Teslascan Enhanced | Exception SPIO-MRI

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0412694
UMLS CUI [1,2]
C0205539
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0024485
UMLS CUI [2,3]
C0675788
UMLS CUI [2,4]
C2349975
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0024485
UMLS CUI [3,3]
C0753357
UMLS CUI [3,4]
C2349975
UMLS CUI [4,1]
C1705847
UMLS CUI [4,2]
C0024485
UMLS CUI [4,3]
C0637607
UMLS CUI [4,4]
C2349975
UMLS CUI [5,1]
C1705847
UMLS CUI [5,2]
C3896586
patients who are clinically unstable and whose clinical course is unpredictable (e.g. due to previous surgery, acute myocardial infarction)
Beskrivning

Patients Unstable Due to Operative Surgical Procedures | Patients Unstable Due to Myocardial Infarction

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0443343
UMLS CUI [1,3]
C0678226
UMLS CUI [1,4]
C0543467
UMLS CUI [2,1]
C0030705
UMLS CUI [2,2]
C0443343
UMLS CUI [2,3]
C0678226
UMLS CUI [2,4]
C0027051
patients with known anaphylactoid or anaphylactic reaction to any contrast media or hypersensitivity to any allergen including drugs
Beskrivning

Anaphylactoid reaction Contrast Media | Anaphylaxis Contrast Media | Drug Allergy Allergen

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0340865
UMLS CUI [1,2]
C0009924
UMLS CUI [2,1]
C0002792
UMLS CUI [2,2]
C0009924
UMLS CUI [3]
C1548333
patients with a contraindication for mri or ct.
Beskrivning

Medical contraindication MRI | Medical contraindication CT

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0024485
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0040405
patients with severe renal impairment (egfr < 30ml/min/1.73m2) or patients on dialysis
Beskrivning

Renal Insufficiency Severe | Estimated Glomerular Filtration Rate | Dialysis

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1565489
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C3811844
UMLS CUI [3]
C0011946
Tillbaka till toppen

Similar models

Eligibility Colorectal Neoplasms NCT00764621

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Secondary malignant neoplasm of liver Secondary to Colorectal Carcinoma | Secondary malignant neoplasm of liver Suspected Secondary to Colorectal Carcinoma | Contrast Enhanced CT Scheduled
Item
patients with known or suspected metachronous liver metastases secondary to colorectal cancer who are scheduled for further contrast-enhanced tomographic imaging
boolean
C0494165 (UMLS CUI [1,1])
C0175668 (UMLS CUI [1,2])
C0009402 (UMLS CUI [1,3])
C0494165 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
C0175668 (UMLS CUI [2,3])
C0009402 (UMLS CUI [2,4])
C1512095 (UMLS CUI [3,1])
C0205539 (UMLS CUI [3,2])
Item Group
C0680251 (UMLS CUI)
Age
Item
patients (men or women) under 18 years of age
boolean
C0001779 (UMLS CUI [1])
Contrast Media Received | Contrast Media Scheduled
Item
patients who have received any contrast material within 24 hours before injection of study drug, or who are scheduled to receive any contrast material within 24 hours after injection
boolean
C0009924 (UMLS CUI [1,1])
C1514756 (UMLS CUI [1,2])
C0009924 (UMLS CUI [2,1])
C0205539 (UMLS CUI [2,2])
Ineligibility Contrast Media Injection
Item
patients not eligible to contrast media (cm) injection according to product labeling
boolean
C1512714 (UMLS CUI [1,1])
C0009924 (UMLS CUI [1,2])
C1533685 (UMLS CUI [1,3])
Pregnancy | Breast Feeding | Childbearing Potential Urine pregnancy test negative Lacking
Item
women who are pregnant, lactating or who are of childbearing potential and have not had a negative urine pregnancy test at baseline visit(s)
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C3831118 (UMLS CUI [3,1])
C0430057 (UMLS CUI [3,2])
C0332268 (UMLS CUI [3,3])
MRI of Liver Scheduled | Exception MRI Eovist Enhanced | Exception MRI MultiHance Enhanced | Exception MRI Teslascan Enhanced | Exception SPIO-MRI
Item
patients scheduled for liver-specific mri other than primovist-enhanced mri, i.e. multihance-, teslascan- or spio-enhanced mri
boolean
C0412694 (UMLS CUI [1,1])
C0205539 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0024485 (UMLS CUI [2,2])
C0675788 (UMLS CUI [2,3])
C2349975 (UMLS CUI [2,4])
C1705847 (UMLS CUI [3,1])
C0024485 (UMLS CUI [3,2])
C0753357 (UMLS CUI [3,3])
C2349975 (UMLS CUI [3,4])
C1705847 (UMLS CUI [4,1])
C0024485 (UMLS CUI [4,2])
C0637607 (UMLS CUI [4,3])
C2349975 (UMLS CUI [4,4])
C1705847 (UMLS CUI [5,1])
C3896586 (UMLS CUI [5,2])
Patients Unstable Due to Operative Surgical Procedures | Patients Unstable Due to Myocardial Infarction
Item
patients who are clinically unstable and whose clinical course is unpredictable (e.g. due to previous surgery, acute myocardial infarction)
boolean
C0030705 (UMLS CUI [1,1])
C0443343 (UMLS CUI [1,2])
C0678226 (UMLS CUI [1,3])
C0543467 (UMLS CUI [1,4])
C0030705 (UMLS CUI [2,1])
C0443343 (UMLS CUI [2,2])
C0678226 (UMLS CUI [2,3])
C0027051 (UMLS CUI [2,4])
Anaphylactoid reaction Contrast Media | Anaphylaxis Contrast Media | Drug Allergy Allergen
Item
patients with known anaphylactoid or anaphylactic reaction to any contrast media or hypersensitivity to any allergen including drugs
boolean
C0340865 (UMLS CUI [1,1])
C0009924 (UMLS CUI [1,2])
C0002792 (UMLS CUI [2,1])
C0009924 (UMLS CUI [2,2])
C1548333 (UMLS CUI [3])
Medical contraindication MRI | Medical contraindication CT
Item
patients with a contraindication for mri or ct.
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0040405 (UMLS CUI [2,2])
Renal Insufficiency Severe | Estimated Glomerular Filtration Rate | Dialysis
Item
patients with severe renal impairment (egfr < 30ml/min/1.73m2) or patients on dialysis
boolean
C1565489 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C3811844 (UMLS CUI [2])
C0011946 (UMLS CUI [3])
Tillbaka till toppen 

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