ID

34783

Descripción

Multimodality Prediction of Success of Atrial Fibrillation Rhythm Control Strategy; ODM derived from: https://clinicaltrials.gov/show/NCT02009683

Link

https://clinicaltrials.gov/show/NCT02009683

Palabras clave

Versiones (1)
  1. 28/1/19 28/1/19 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

28 de enero de 2019

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT02009683

Inglés

Eligibility Atrial Fibrillation NCT02009683

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
haemodynamic stable patients with persistent af scheduled for dcc.
Descripción

Hemodynamics Stable | Persistent atrial fibrillation | Direct current cardioversion Scheduled

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0019010
UMLS CUI [1,2]
C0205360
UMLS CUI [2]
C2585653
UMLS CUI [3,1]
C0542380
UMLS CUI [3,2]
C0205539
written informed consent.
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
patients > 18 years old.
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
atrial flutter at time of dcc.
Descripción

Atrial Flutter

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0004239
patients with known oesophageal disease.
Descripción

Esophageal Disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0014852
patients with previous operations on throat or oesophagus.
Descripción

Throat surgery | Operation on esophagus

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0749390
UMLS CUI [2]
C0192259
postoperative atrial fibrillation.
Descripción

Atrial Fibrillation Postoperative

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0032790
patients with previous ablation for af.
Descripción

Catheter ablation for atrial fibrillation Previous

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2702800
UMLS CUI [1,2]
C0205156
previous inclusion in this study.
Descripción

Study Subject Participation Status | Enrollment Previous

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C1516879
UMLS CUI [2,2]
C0205156
patients on anti-arrhythmic drugs (aad).
Descripción

Anti-Arrhythmia Agents

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0003195
patients with pacemakers unable to detect af and with a regular paced rhythm during af.
Descripción

Artificial cardiac pacemaker Inappropriate Detection Atrial Fibrillation | Paced Rhythm Regular During Atrial Fibrillation

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0030163
UMLS CUI [1,2]
C1548788
UMLS CUI [1,3]
C1511790
UMLS CUI [1,4]
C0004238
UMLS CUI [2,1]
C2981711
UMLS CUI [2,2]
C0205272
UMLS CUI [2,3]
C0347984
UMLS CUI [2,4]
C0004238
planned ablation for af.
Descripción

Catheter ablation for atrial fibrillation Planned

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2702800
UMLS CUI [1,2]
C1301732
myocardial infarction within the last 4 weeks.
Descripción

Myocardial Infarction

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0027051
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Similar models

Eligibility Atrial Fibrillation NCT02009683

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Hemodynamics Stable | Persistent atrial fibrillation | Direct current cardioversion Scheduled
Item
haemodynamic stable patients with persistent af scheduled for dcc.
boolean
C0019010 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C2585653 (UMLS CUI [2])
C0542380 (UMLS CUI [3,1])
C0205539 (UMLS CUI [3,2])
Informed Consent
Item
written informed consent.
boolean
C0021430 (UMLS CUI [1])
Age
Item
patients > 18 years old.
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Atrial Flutter
Item
atrial flutter at time of dcc.
boolean
C0004239 (UMLS CUI [1])
Esophageal Disease
Item
patients with known oesophageal disease.
boolean
C0014852 (UMLS CUI [1])
Throat surgery | Operation on esophagus
Item
patients with previous operations on throat or oesophagus.
boolean
C0749390 (UMLS CUI [1])
C0192259 (UMLS CUI [2])
Atrial Fibrillation Postoperative
Item
postoperative atrial fibrillation.
boolean
C0004238 (UMLS CUI [1,1])
C0032790 (UMLS CUI [1,2])
Catheter ablation for atrial fibrillation Previous
Item
patients with previous ablation for af.
boolean
C2702800 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
Study Subject Participation Status | Enrollment Previous
Item
previous inclusion in this study.
boolean
C2348568 (UMLS CUI [1])
C1516879 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
Anti-Arrhythmia Agents
Item
patients on anti-arrhythmic drugs (aad).
boolean
C0003195 (UMLS CUI [1])
Artificial cardiac pacemaker Inappropriate Detection Atrial Fibrillation | Paced Rhythm Regular During Atrial Fibrillation
Item
patients with pacemakers unable to detect af and with a regular paced rhythm during af.
boolean
C0030163 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
C1511790 (UMLS CUI [1,3])
C0004238 (UMLS CUI [1,4])
C2981711 (UMLS CUI [2,1])
C0205272 (UMLS CUI [2,2])
C0347984 (UMLS CUI [2,3])
C0004238 (UMLS CUI [2,4])
Catheter ablation for atrial fibrillation Planned
Item
planned ablation for af.
boolean
C2702800 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
Myocardial Infarction
Item
myocardial infarction within the last 4 weeks.
boolean
C0027051 (UMLS CUI [1])
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