ID

44745

Beskrivning

Renal Artery Contrast-Free Trial; ODM derived from: https://clinicaltrials.gov/show/NCT01576835

Länk

https://clinicaltrials.gov/show/NCT01576835

Nyckelord

Versioner (1)
  1. 2021-11-10 2021-11-10 -
Rättsinnehavare

Central Coast Cardiovascular Research

Uppladdad den

10 november 2021

DOI

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Licens

Creative Commons BY-NC 4.0
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Eligibility Renal Artery Stenosis NCT01576835

Engelsk

Eligibility Renal Artery Stenosis NCT01576835

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
the abdominal cta evaluation form has been completed and confirmed to fit criteria for study enrollment
Beskrivning

abdominal ct angiography evaluation form has been completed and confirmed to fit criteria for study enrollment

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1536105
UMLS CUI [1,2]
C0000726
UMLS CUI [1,3]
C0220825
UMLS CUI [1,4]
C0376315
UMLS CUI [1,5]
C1516637
the research mra will be completed within 3 months of abdominal cta
Beskrivning

research mr angiography will be completed within 3 months of abdominal cta

Datatyp

boolean

Alias
UMLS CUI [1,1]
C3891069
UMLS CUI [1,2]
C0008972
UMLS CUI [1,3]
C0205197
UMLS CUI [1,4]
C0449238
UMLS CUI [1,5]
C1536105
UMLS CUI [1,6]
C0000726
subject signed and dated the informed consent form
Beskrivning

signed and dated informed consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0742766
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0011008
subject agrees to a "research" abdominal mra
Beskrivning

agreement to research abdominal mr angiography

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0680240
UMLS CUI [1,2]
C3891069
UMLS CUI [1,3]
C0000726
UMLS CUI [1,4]
C0008972
subject is able to follow breathing and scanning instructions
Beskrivning

ability to follow breathing and scanning instructions

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0085732
UMLS CUI [1,2]
C1442085
UMLS CUI [1,3]
C0035203
UMLS CUI [2,1]
C0085732
UMLS CUI [2,2]
C1442085
UMLS CUI [2,3]
C0441633
subject is at least 18 years of age
Beskrivning

subject is at least 18 years of age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
subject has had a significant change in clinical condition between the time of abdominal cta and abdominal mra (e.g. worsening renal function, renal vascular intervention)
Beskrivning

significant change in clinical condition between the time of abdominal cta and abdominal mra (e.g. worsening renal function, renal vascular intervention)

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0348080
UMLS CUI [1,2]
C0392747
UMLS CUI [1,3]
C2348792
UMLS CUI [1,4]
C1536105
UMLS CUI [1,5]
C3891069
UMLS CUI [1,6]
C0000726
UMLS CUI [1,7]
C0232804
UMLS CUI [1,8]
C1457868
UMLS CUI [1,9]
C0268790
subject has renal stents, or other known material that may affect mr image quality
Beskrivning

renal stents or other material affecting mr image quality

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1322812
UMLS CUI [1,2]
C0024485
UMLS CUI [1,3]
C0806487
UMLS CUI [2,1]
C0520510
UMLS CUI [2,2]
C0024485
UMLS CUI [2,3]
C0806487
subject has a contraindication to an mri
Beskrivning

contraindication to mri

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0024485
subject had intravenous gadolinium media within the previous 24 hours
Beskrivning

intravenous gadolinium media within the previous 24 hours

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0009924
UMLS CUI [1,2]
C0060933
UMLS CUI [1,3]
C1522726
UMLS CUI [1,4]
C0332185
subject has a baseline heart rate >90 beats per minute or respiratory rate >25 breaths/minute
Beskrivning

baseline heart rate >90 beats per minute or respiratory rate >25 breaths/minute

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1442488
UMLS CUI [1,2]
C0018810
UMLS CUI [1,3]
C0750480
UMLS CUI [2,1]
C1442488
UMLS CUI [2,2]
C0231832
UMLS CUI [2,3]
C0750480
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Similar models

Eligibility Renal Artery Stenosis NCT01576835

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
abdominal ct angiography evaluation form has been completed and confirmed to fit criteria for study enrollment
Item
the abdominal cta evaluation form has been completed and confirmed to fit criteria for study enrollment
boolean
C1536105 (UMLS CUI [1,1])
C0000726 (UMLS CUI [1,2])
C0220825 (UMLS CUI [1,3])
C0376315 (UMLS CUI [1,4])
C1516637 (UMLS CUI [1,5])
research mr angiography will be completed within 3 months of abdominal cta
Item
the research mra will be completed within 3 months of abdominal cta
boolean
C3891069 (UMLS CUI [1,1])
C0008972 (UMLS CUI [1,2])
C0205197 (UMLS CUI [1,3])
C0449238 (UMLS CUI [1,4])
C1536105 (UMLS CUI [1,5])
C0000726 (UMLS CUI [1,6])
signed and dated informed consent
Item
subject signed and dated the informed consent form
boolean
C0742766 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C0011008 (UMLS CUI [2,2])
agreement to research abdominal mr angiography
Item
subject agrees to a "research" abdominal mra
boolean
C0680240 (UMLS CUI [1,1])
C3891069 (UMLS CUI [1,2])
C0000726 (UMLS CUI [1,3])
C0008972 (UMLS CUI [1,4])
ability to follow breathing and scanning instructions
Item
subject is able to follow breathing and scanning instructions
boolean
C0085732 (UMLS CUI [1,1])
C1442085 (UMLS CUI [1,2])
C0035203 (UMLS CUI [1,3])
C0085732 (UMLS CUI [2,1])
C1442085 (UMLS CUI [2,2])
C0441633 (UMLS CUI [2,3])
subject is at least 18 years of age
Item
subject is at least 18 years of age
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
significant change in clinical condition between the time of abdominal cta and abdominal mra (e.g. worsening renal function, renal vascular intervention)
Item
subject has had a significant change in clinical condition between the time of abdominal cta and abdominal mra (e.g. worsening renal function, renal vascular intervention)
boolean
C0348080 (UMLS CUI [1,1])
C0392747 (UMLS CUI [1,2])
C2348792 (UMLS CUI [1,3])
C1536105 (UMLS CUI [1,4])
C3891069 (UMLS CUI [1,5])
C0000726 (UMLS CUI [1,6])
C0232804 (UMLS CUI [1,7])
C1457868 (UMLS CUI [1,8])
C0268790 (UMLS CUI [1,9])
renal stents or other material affecting mr image quality
Item
subject has renal stents, or other known material that may affect mr image quality
boolean
C1322812 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
C0806487 (UMLS CUI [1,3])
C0520510 (UMLS CUI [2,1])
C0024485 (UMLS CUI [2,2])
C0806487 (UMLS CUI [2,3])
contraindication to mri
Item
subject has a contraindication to an mri
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
intravenous gadolinium media within the previous 24 hours
Item
subject had intravenous gadolinium media within the previous 24 hours
boolean
C0009924 (UMLS CUI [1,1])
C0060933 (UMLS CUI [1,2])
C1522726 (UMLS CUI [1,3])
C0332185 (UMLS CUI [1,4])
baseline heart rate >90 beats per minute or respiratory rate >25 breaths/minute
Item
subject has a baseline heart rate >90 beats per minute or respiratory rate >25 breaths/minute
boolean
C1442488 (UMLS CUI [1,1])
C0018810 (UMLS CUI [1,2])
C0750480 (UMLS CUI [1,3])
C1442488 (UMLS CUI [2,1])
C0231832 (UMLS CUI [2,2])
C0750480 (UMLS CUI [2,3])
Tillbaka till toppen 

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