ID

25866

Beschrijving

The Effect of Short Term Amiodarone Treatment After Catheter Ablation for Atrial Fibrillation; ODM derived from: https://clinicaltrials.gov/show/NCT00826826

Link

https://clinicaltrials.gov/show/NCT00826826

Trefwoorden

Versies (1)
  1. 22-09-17 22-09-17 -
Geüploaded op

22 september 2017

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT00826826

Engels

Eligibility Atrial Fibrillation NCT00826826

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with symptomatic paroxysmal or persistent atrial fibrillation undergoing catheter ablation for atrial fibrillation. (persistent episodes may last no more than 12 months)
Beschrijving

Paroxysmal atrial fibrillation Symptomatic | Persistent atrial fibrillation Symptomatic | Catheter ablation for atrial fibrillation | Episode persistent Duration

Datatype

boolean

Alias
UMLS CUI [1,1]
C0235480
UMLS CUI [1,2]
C0231220
UMLS CUI [2,1]
C2585653
UMLS CUI [2,2]
C0231220
UMLS CUI [3]
C2702800
UMLS CUI [4,1]
C0332189
UMLS CUI [4,2]
C0205322
UMLS CUI [4,3]
C0449238
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
contraindication or intolerance to amiodarone.
Beschrijving

Medical contraindication Amiodarone | Intolerance to Amiodarone

Datatype

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0002598
UMLS CUI [2,1]
C1744706
UMLS CUI [2,2]
C0002598
prolonged amiodarone treatment within 3 months before the planned ablation procedure.
Beschrijving

Amiodarone Prolonged

Datatype

boolean

Alias
UMLS CUI [1,1]
C0002598
UMLS CUI [1,2]
C0439590
previous participation in this study.
Beschrijving

Study Subject Participation Status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
other cardiac arrythmias (patients with co-existing atrial flutter can be included).
Beschrijving

Cardiac Arrhythmia | Atrial Flutter Concurrent allowed

Datatype

boolean

Alias
UMLS CUI [1]
C0003811
UMLS CUI [2,1]
C0004239
UMLS CUI [2,2]
C0205420
UMLS CUI [2,3]
C0683607
antiarrhythmic treatment for indication other than atrial fibrillation (or atrial flutter).
Beschrijving

Anti-Arrhythmia Agents | Indication Other

Datatype

boolean

Alias
UMLS CUI [1]
C0003195
UMLS CUI [2,1]
C3146298
UMLS CUI [2,2]
C0205394
heart failure (nyha class iii or iv or left ventricular ejection fraction < 35%).
Beschrijving

Heart failure New York Heart Association Classification | Left ventricular ejection fraction

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1275491
UMLS CUI [2]
C0428772
significant heart valve disease.
Beschrijving

Heart valve disease

Datatype

boolean

Alias
UMLS CUI [1]
C0018824
significant lung disease, thyroid dysfunction or liver disease.
Beschrijving

Lung diseases | Thyroid dysfunction | Liver diseases

Datatype

boolean

Alias
UMLS CUI [1]
C0024115
UMLS CUI [2]
C0348024
UMLS CUI [3]
C0023895
inability or unwillingness to be treated with anticoagulation before and during the study.
Beschrijving

Anticoagulation Therapy Unable | Anticoagulation Therapy Unwilling

Datatype

boolean

Alias
UMLS CUI [1,1]
C0003281
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0003281
UMLS CUI [2,2]
C0558080
females with birth giving potential
Beschrijving

Childbearing Potential

Datatype

boolean

Alias
UMLS CUI [1]
C3831118
failure to give informed concent.
Beschrijving

Informed Consent failed

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0231175
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Similar models

Eligibility Atrial Fibrillation NCT00826826

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Paroxysmal atrial fibrillation Symptomatic | Persistent atrial fibrillation Symptomatic | Catheter ablation for atrial fibrillation | Episode persistent Duration
Item
patients with symptomatic paroxysmal or persistent atrial fibrillation undergoing catheter ablation for atrial fibrillation. (persistent episodes may last no more than 12 months)
boolean
C0235480 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C2585653 (UMLS CUI [2,1])
C0231220 (UMLS CUI [2,2])
C2702800 (UMLS CUI [3])
C0332189 (UMLS CUI [4,1])
C0205322 (UMLS CUI [4,2])
C0449238 (UMLS CUI [4,3])
Item Group
C0680251 (UMLS CUI)
Medical contraindication Amiodarone | Intolerance to Amiodarone
Item
contraindication or intolerance to amiodarone.
boolean
C1301624 (UMLS CUI [1,1])
C0002598 (UMLS CUI [1,2])
C1744706 (UMLS CUI [2,1])
C0002598 (UMLS CUI [2,2])
Amiodarone Prolonged
Item
prolonged amiodarone treatment within 3 months before the planned ablation procedure.
boolean
C0002598 (UMLS CUI [1,1])
C0439590 (UMLS CUI [1,2])
Study Subject Participation Status
Item
previous participation in this study.
boolean
C2348568 (UMLS CUI [1])
Cardiac Arrhythmia | Atrial Flutter Concurrent allowed
Item
other cardiac arrythmias (patients with co-existing atrial flutter can be included).
boolean
C0003811 (UMLS CUI [1])
C0004239 (UMLS CUI [2,1])
C0205420 (UMLS CUI [2,2])
C0683607 (UMLS CUI [2,3])
Anti-Arrhythmia Agents | Indication Other
Item
antiarrhythmic treatment for indication other than atrial fibrillation (or atrial flutter).
boolean
C0003195 (UMLS CUI [1])
C3146298 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
Heart failure New York Heart Association Classification | Left ventricular ejection fraction
Item
heart failure (nyha class iii or iv or left ventricular ejection fraction < 35%).
boolean
C0018801 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
C0428772 (UMLS CUI [2])
Heart valve disease
Item
significant heart valve disease.
boolean
C0018824 (UMLS CUI [1])
Lung diseases | Thyroid dysfunction | Liver diseases
Item
significant lung disease, thyroid dysfunction or liver disease.
boolean
C0024115 (UMLS CUI [1])
C0348024 (UMLS CUI [2])
C0023895 (UMLS CUI [3])
Anticoagulation Therapy Unable | Anticoagulation Therapy Unwilling
Item
inability or unwillingness to be treated with anticoagulation before and during the study.
boolean
C0003281 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0003281 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
Childbearing Potential
Item
females with birth giving potential
boolean
C3831118 (UMLS CUI [1])
Informed Consent failed
Item
failure to give informed concent.
boolean
C0021430 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
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