ID

37472

Description

DECAAF: Delayed-Enhancement MRI (DE-MRI) Determinant of Successful Radiofrequency Catheter Ablation of Atrial Fibrillation; ODM derived from: https://clinicaltrials.gov/show/NCT01150214

Lien

https://clinicaltrials.gov/show/NCT01150214

Mots-clés

Versions (1)
  1. 30/07/2019 30/07/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

30 juillet 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT01150214

Anglais

Eligibility Atrial Fibrillation NCT01150214

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients who underwent an af ablation as per recent heart rhythm society (hrs) consensus document, as per the university of utah afib database (irb_00020347)
Description

Catheter ablation for atrial fibrillation

Type de données

boolean

Alias
UMLS CUI [1]
C2702800
patients who have had an mri post-ablation.
Description

MRI Post Ablation

Type de données

boolean

Alias
UMLS CUI [1,1]
C0024485
UMLS CUI [1,2]
C0687676
UMLS CUI [1,3]
C0547070
age ≥18 years.
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
contraindication for de-mri with a full dose of gadolinium-based contrast agent.
Description

Medical contraindication MRI | Gadolinium-based Contrast Agent Dose Full

Type de données

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0024485
UMLS CUI [2,1]
C3249258
UMLS CUI [2,2]
C0178602
UMLS CUI [2,3]
C0443225
previous left atrial ablation or surgical procedure
Description

Left atrium Ablation | Left atrium Operative Surgical Procedure

Type de données

boolean

Alias
UMLS CUI [1,1]
C0225860
UMLS CUI [1,2]
C0547070
UMLS CUI [2,1]
C0225860
UMLS CUI [2,2]
C0543467
renal failure with crcl <60 ml/min
Description

Kidney Failure | Creatinine clearance measurement

Type de données

boolean

Alias
UMLS CUI [1]
C0035078
UMLS CUI [2]
C0373595
women currently pregnant, breastfeeding, or of childbearing age not currently taking or not willing to use a reliable form of contraception
Description

Pregnancy | Breast Feeding | Childbearing Potential Contraceptive methods Absent | Childbearing Potential Contraceptive methods Unwilling

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3,1]
C3831118
UMLS CUI [3,2]
C0700589
UMLS CUI [3,3]
C0332197
UMLS CUI [4,1]
C3831118
UMLS CUI [4,2]
C0700589
UMLS CUI [4,3]
C0558080
mental or physical inability to take part in the study
Description

Study Subject Participation Status Unable | Mental handicap | Physical disability

Type de données

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C1299582
UMLS CUI [2]
C1306341
UMLS CUI [3]
C0520817
uncontrolled hypertension
Description

Uncontrolled hypertension

Type de données

boolean

Alias
UMLS CUI [1]
C1868885
morbid obesity (bmi > 35), or inability to be placed in mri due to body mass.
Description

Obesity, Morbid | Body mass index | MRI Unsuccessful Due to Body mass

Type de données

boolean

Alias
UMLS CUI [1]
C0028756
UMLS CUI [2]
C1305855
UMLS CUI [3,1]
C0024485
UMLS CUI [3,2]
C1272705
UMLS CUI [3,3]
C0678226
UMLS CUI [3,4]
C0518010
patients who have not had a de-mri post-ablation.
Description

Absence MRI Post Ablation

Type de données

boolean

Alias
UMLS CUI [1,1]
C0332197
UMLS CUI [1,2]
C0024485
UMLS CUI [1,3]
C0687676
UMLS CUI [1,4]
C0547070
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Eligibility Atrial Fibrillation NCT01150214

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Catheter ablation for atrial fibrillation
Item
patients who underwent an af ablation as per recent heart rhythm society (hrs) consensus document, as per the university of utah afib database (irb_00020347)
boolean
C2702800 (UMLS CUI [1])
MRI Post Ablation
Item
patients who have had an mri post-ablation.
boolean
C0024485 (UMLS CUI [1,1])
C0687676 (UMLS CUI [1,2])
C0547070 (UMLS CUI [1,3])
Age
Item
age ≥18 years.
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Medical contraindication MRI | Gadolinium-based Contrast Agent Dose Full
Item
contraindication for de-mri with a full dose of gadolinium-based contrast agent.
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
C3249258 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C0443225 (UMLS CUI [2,3])
Left atrium Ablation | Left atrium Operative Surgical Procedure
Item
previous left atrial ablation or surgical procedure
boolean
C0225860 (UMLS CUI [1,1])
C0547070 (UMLS CUI [1,2])
C0225860 (UMLS CUI [2,1])
C0543467 (UMLS CUI [2,2])
Kidney Failure | Creatinine clearance measurement
Item
renal failure with crcl <60 ml/min
boolean
C0035078 (UMLS CUI [1])
C0373595 (UMLS CUI [2])
Pregnancy | Breast Feeding | Childbearing Potential Contraceptive methods Absent | Childbearing Potential Contraceptive methods Unwilling
Item
women currently pregnant, breastfeeding, or of childbearing age not currently taking or not willing to use a reliable form of contraception
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C3831118 (UMLS CUI [3,1])
C0700589 (UMLS CUI [3,2])
C0332197 (UMLS CUI [3,3])
C3831118 (UMLS CUI [4,1])
C0700589 (UMLS CUI [4,2])
C0558080 (UMLS CUI [4,3])
Study Subject Participation Status Unable | Mental handicap | Physical disability
Item
mental or physical inability to take part in the study
boolean
C2348568 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C1306341 (UMLS CUI [2])
C0520817 (UMLS CUI [3])
Uncontrolled hypertension
Item
uncontrolled hypertension
boolean
C1868885 (UMLS CUI [1])
Obesity, Morbid | Body mass index | MRI Unsuccessful Due to Body mass
Item
morbid obesity (bmi > 35), or inability to be placed in mri due to body mass.
boolean
C0028756 (UMLS CUI [1])
C1305855 (UMLS CUI [2])
C0024485 (UMLS CUI [3,1])
C1272705 (UMLS CUI [3,2])
C0678226 (UMLS CUI [3,3])
C0518010 (UMLS CUI [3,4])
Absence MRI Post Ablation
Item
patients who have not had a de-mri post-ablation.
boolean
C0332197 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
C0687676 (UMLS CUI [1,3])
C0547070 (UMLS CUI [1,4])
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