ID

20392

Description

Siemens 3-D C-Arm CT of the Heart Chambers; ODM derived from: https://clinicaltrials.gov/show/NCT00619450

Lien

https://clinicaltrials.gov/show/NCT00619450

Mots-clés

  1. 21/02/2017 21/02/2017 -
Téléchargé le

21 février 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Atrial Fibrillation NCT00619450

Eligibility Atrial Fibrillation NCT00619450

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients undergoing ep diagnostic or therapeutic procedure
Description

Cardiac Electrophysiology; Catheter, electrophysiology, diagnostic/ablation

Type de données

boolean

Alias
UMLS CUI [1,1]
C0430467
UMLS CUI [1,2]
C0993742
age > 18 years
Description

age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
male or female
Description

gender

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
weight < 250 lbs
Description

body weight

Type de données

boolean

Alias
UMLS CUI [1]
C0005910
not pregnant - women without childbearing potential or women consenting to a pregnancy test
Description

pregnancy, childbearing potential

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C3831118
able to hold breath for a maximum of 15 seconds
Description

able to hold breath

Type de données

boolean

Alias
UMLS CUI [1,1]
C0235744
UMLS CUI [1,2]
C0085732
sufficient kidney function to support a maximum of 200 cc of contrast in addition to whatever contrast will be given during the ep procedure
Description

renal function, contrast agent

Type de données

boolean

Alias
UMLS CUI [1]
C0232804
UMLS CUI [2]
C0009924
creatinine < 1.7 and cleared by physician prior to case
Description

creatinine

Type de données

boolean

Alias
UMLS CUI [1]
C0201976
implantable foreign objects acceptable
Description

implantable foreign objects

Type de données

boolean

Alias
UMLS CUI [1]
C2828363
nsr or af
Description

normal sinus rhythm or atrial fibrillation

Type de données

boolean

Alias
UMLS CUI [1]
C0232202
UMLS CUI [2]
C0004238
patient must sign an informed consent
Description

informed consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients should not have undergone a ct or cta scan in the 24 hours prior to this study.
Description

ct or cta scan

Type de données

boolean

Alias
UMLS CUI [1]
C0040405
UMLS CUI [2]
C1536105
creatinine (gfr value) greater than 60
Description

creatinine

Type de données

boolean

Alias
UMLS CUI [1]
C0201976

Similar models

Eligibility Atrial Fibrillation NCT00619450

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Cardiac Electrophysiology; Catheter, electrophysiology, diagnostic/ablation
Item
patients undergoing ep diagnostic or therapeutic procedure
boolean
C0430467 (UMLS CUI [1,1])
C0993742 (UMLS CUI [1,2])
age
Item
age > 18 years
boolean
C0001779 (UMLS CUI [1])
gender
Item
male or female
boolean
C0079399 (UMLS CUI [1])
body weight
Item
weight < 250 lbs
boolean
C0005910 (UMLS CUI [1])
pregnancy, childbearing potential
Item
not pregnant - women without childbearing potential or women consenting to a pregnancy test
boolean
C0032961 (UMLS CUI [1])
C3831118 (UMLS CUI [2])
able to hold breath
Item
able to hold breath for a maximum of 15 seconds
boolean
C0235744 (UMLS CUI [1,1])
C0085732 (UMLS CUI [1,2])
renal function, contrast agent
Item
sufficient kidney function to support a maximum of 200 cc of contrast in addition to whatever contrast will be given during the ep procedure
boolean
C0232804 (UMLS CUI [1])
C0009924 (UMLS CUI [2])
creatinine
Item
creatinine < 1.7 and cleared by physician prior to case
boolean
C0201976 (UMLS CUI [1])
implantable foreign objects
Item
implantable foreign objects acceptable
boolean
C2828363 (UMLS CUI [1])
normal sinus rhythm or atrial fibrillation
Item
nsr or af
boolean
C0232202 (UMLS CUI [1])
C0004238 (UMLS CUI [2])
informed consent
Item
patient must sign an informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
ct or cta scan
Item
patients should not have undergone a ct or cta scan in the 24 hours prior to this study.
boolean
C0040405 (UMLS CUI [1])
C1536105 (UMLS CUI [2])
creatinine
Item
creatinine (gfr value) greater than 60
boolean
C0201976 (UMLS CUI [1])

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