ID

37454

Description

The RECORD Asia-Pacific Atrial Fibrillation Registry; ODM derived from: https://clinicaltrials.gov/show/NCT00995748

Lien

https://clinicaltrials.gov/show/NCT00995748

Mots-clés

Versions (1)
  1. 29/07/2019 29/07/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

29 juillet 2019

DOI

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Licence

Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT00995748

Anglais

Eligibility Atrial Fibrillation NCT00995748

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient presenting with either:
Description

Patient condition finding

Type de données

boolean

Alias
UMLS CUI [1]
C1690487
history of atrial fibrillation diagnosed < 1 year by standard electro-cardiogram (ecg) or by ecg-holter monitoring (treated or not or whatever rhythm at inclusion).
Description

Atrial Fibrillation Disease length ECG | Atrial Fibrillation Disease length Holter Electrocardiography | Treatment Present | Treatment Absent | Atrial rhythm Status

Type de données

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0872146
UMLS CUI [1,3]
C0013798
UMLS CUI [2,1]
C0004238
UMLS CUI [2,2]
C0872146
UMLS CUI [2,3]
C0013801
UMLS CUI [3,1]
C0087111
UMLS CUI [3,2]
C0150312
UMLS CUI [4,1]
C0087111
UMLS CUI [4,2]
C0332197
UMLS CUI [5,1]
C0232203
UMLS CUI [5,2]
C0449438
new atrial fibrillation diagnosed by standard ecg or by ecg-holter monitoring at inclusion visit.
Description

Atrial Fibrillation Newly Diagnosed ECG | Atrial Fibrillation Newly Diagnosed Holter Electrocardiography

Type de données

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C1518321
UMLS CUI [1,3]
C0013798
UMLS CUI [2,1]
C0004238
UMLS CUI [2,2]
C1518321
UMLS CUI [2,3]
C0013801
patient eligible for a pharmacological treatment of af (by rhythm or rate control agent).
Description

Pharmacotherapy Atrial Fibrillation | Pharmaceutical Preparations Control Atrial rhythm | Pharmaceutical Preparations Control Heart rate

Type de données

boolean

Alias
UMLS CUI [1,1]
C0013216
UMLS CUI [1,2]
C0004238
UMLS CUI [2,1]
C0013227
UMLS CUI [2,2]
C2587213
UMLS CUI [2,3]
C0232203
UMLS CUI [3,1]
C0013227
UMLS CUI [3,2]
C2587213
UMLS CUI [3,3]
C0018810
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
af due to transient cause (thyrotoxicosis, alcohol intoxication, acute phase of myocardial infarction, pericarditis, myocarditis, electrocution, pulmonary embolism or other pulmonary disease, hydroelectrolytic disorder, metabolic disorder, etc.).
Description

Atrial Fibrillation Due to Cause Transient | Thyrotoxicosis | Alcohol consumption | Myocardial Infarction | Pericarditis | Myocarditis | Electrocution | Pulmonary Embolism | Lung disease | Other Coding | Metabolic Disease

Type de données

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0015127
UMLS CUI [1,4]
C0205374
UMLS CUI [2]
C0040156
UMLS CUI [3]
C0001948
UMLS CUI [4]
C0027051
UMLS CUI [5]
C0031046
UMLS CUI [6]
C0027059
UMLS CUI [7]
C0277644
UMLS CUI [8]
C0034065
UMLS CUI [9]
C0024115
UMLS CUI [10]
C3846158
UMLS CUI [11]
C0025517
post cardiac surgery af (≤3 months).
Description

Atrial Fibrillation Post Cardiac Surgery

Type de données

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0687676
UMLS CUI [1,3]
C0018821
mentally disabled patients unable to understand or sign the written informed consent.
Description

Mental handicap | Informed Consent Unable

Type de données

boolean

Alias
UMLS CUI [1]
C1306341
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C1299582
patients unable to comply with follow-up visits.
Description

Compliance Follow-up visit Unable

Type de données

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0589121
UMLS CUI [1,3]
C1299582
patients with pacemaker, implantable cardioverter defibrillator (icd).
Description

Artificial cardiac pacemaker | Implantable defibrillator

Type de données

boolean

Alias
UMLS CUI [1]
C0030163
UMLS CUI [2]
C0162589
patients scheduled for pulmonary vein ablation, av node/his bundle ablation, or pacemaker implantation.
Description

Pulmonary vein Ablation Scheduled | Ablation of Cardiac AV node Scheduled | Catheter ablation of bundle of His Scheduled | Implantation of cardiac pacemaker Scheduled

Type de données

boolean

Alias
UMLS CUI [1,1]
C0034090
UMLS CUI [1,2]
C0547070
UMLS CUI [1,3]
C0205539
UMLS CUI [2,1]
C3275044
UMLS CUI [2,2]
C0205539
UMLS CUI [3,1]
C2007105
UMLS CUI [3,2]
C0205539
UMLS CUI [4,1]
C0189842
UMLS CUI [4,2]
C0205539
patient included in any clinical trial in the previous 3 months.
Description

Study Subject Participation Status

Type de données

boolean

Alias
UMLS CUI [1]
C2348568
pregnant or breastfeeding women.
Description

Pregnancy | Breast Feeding

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
the above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Description

Study Subject Participation Status | Consideration Additional

Type de données

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C0518609
UMLS CUI [2,2]
C1524062
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Similar models

Eligibility Atrial Fibrillation NCT00995748

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Patient condition finding
Item
patient presenting with either:
boolean
C1690487 (UMLS CUI [1])
Atrial Fibrillation Disease length ECG | Atrial Fibrillation Disease length Holter Electrocardiography | Treatment Present | Treatment Absent | Atrial rhythm Status
Item
history of atrial fibrillation diagnosed < 1 year by standard electro-cardiogram (ecg) or by ecg-holter monitoring (treated or not or whatever rhythm at inclusion).
boolean
C0004238 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
C0013798 (UMLS CUI [1,3])
C0004238 (UMLS CUI [2,1])
C0872146 (UMLS CUI [2,2])
C0013801 (UMLS CUI [2,3])
C0087111 (UMLS CUI [3,1])
C0150312 (UMLS CUI [3,2])
C0087111 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
C0232203 (UMLS CUI [5,1])
C0449438 (UMLS CUI [5,2])
Atrial Fibrillation Newly Diagnosed ECG | Atrial Fibrillation Newly Diagnosed Holter Electrocardiography
Item
new atrial fibrillation diagnosed by standard ecg or by ecg-holter monitoring at inclusion visit.
boolean
C0004238 (UMLS CUI [1,1])
C1518321 (UMLS CUI [1,2])
C0013798 (UMLS CUI [1,3])
C0004238 (UMLS CUI [2,1])
C1518321 (UMLS CUI [2,2])
C0013801 (UMLS CUI [2,3])
Pharmacotherapy Atrial Fibrillation | Pharmaceutical Preparations Control Atrial rhythm | Pharmaceutical Preparations Control Heart rate
Item
patient eligible for a pharmacological treatment of af (by rhythm or rate control agent).
boolean
C0013216 (UMLS CUI [1,1])
C0004238 (UMLS CUI [1,2])
C0013227 (UMLS CUI [2,1])
C2587213 (UMLS CUI [2,2])
C0232203 (UMLS CUI [2,3])
C0013227 (UMLS CUI [3,1])
C2587213 (UMLS CUI [3,2])
C0018810 (UMLS CUI [3,3])
Item Group
C0680251 (UMLS CUI)
Atrial Fibrillation Due to Cause Transient | Thyrotoxicosis | Alcohol consumption | Myocardial Infarction | Pericarditis | Myocarditis | Electrocution | Pulmonary Embolism | Lung disease | Other Coding | Metabolic Disease
Item
af due to transient cause (thyrotoxicosis, alcohol intoxication, acute phase of myocardial infarction, pericarditis, myocarditis, electrocution, pulmonary embolism or other pulmonary disease, hydroelectrolytic disorder, metabolic disorder, etc.).
boolean
C0004238 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0015127 (UMLS CUI [1,3])
C0205374 (UMLS CUI [1,4])
C0040156 (UMLS CUI [2])
C0001948 (UMLS CUI [3])
C0027051 (UMLS CUI [4])
C0031046 (UMLS CUI [5])
C0027059 (UMLS CUI [6])
C0277644 (UMLS CUI [7])
C0034065 (UMLS CUI [8])
C0024115 (UMLS CUI [9])
C3846158 (UMLS CUI [10])
C0025517 (UMLS CUI [11])
Atrial Fibrillation Post Cardiac Surgery
Item
post cardiac surgery af (≤3 months).
boolean
C0004238 (UMLS CUI [1,1])
C0687676 (UMLS CUI [1,2])
C0018821 (UMLS CUI [1,3])
Mental handicap | Informed Consent Unable
Item
mentally disabled patients unable to understand or sign the written informed consent.
boolean
C1306341 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
Compliance Follow-up visit Unable
Item
patients unable to comply with follow-up visits.
boolean
C1321605 (UMLS CUI [1,1])
C0589121 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
Artificial cardiac pacemaker | Implantable defibrillator
Item
patients with pacemaker, implantable cardioverter defibrillator (icd).
boolean
C0030163 (UMLS CUI [1])
C0162589 (UMLS CUI [2])
Pulmonary vein Ablation Scheduled | Ablation of Cardiac AV node Scheduled | Catheter ablation of bundle of His Scheduled | Implantation of cardiac pacemaker Scheduled
Item
patients scheduled for pulmonary vein ablation, av node/his bundle ablation, or pacemaker implantation.
boolean
C0034090 (UMLS CUI [1,1])
C0547070 (UMLS CUI [1,2])
C0205539 (UMLS CUI [1,3])
C3275044 (UMLS CUI [2,1])
C0205539 (UMLS CUI [2,2])
C2007105 (UMLS CUI [3,1])
C0205539 (UMLS CUI [3,2])
C0189842 (UMLS CUI [4,1])
C0205539 (UMLS CUI [4,2])
Study Subject Participation Status
Item
patient included in any clinical trial in the previous 3 months.
boolean
C2348568 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnant or breastfeeding women.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Study Subject Participation Status | Consideration Additional
Item
the above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
boolean
C2348568 (UMLS CUI [1])
C0518609 (UMLS CUI [2,1])
C1524062 (UMLS CUI [2,2])
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