ID

37587

Description

Persistent Atrial Fibrillation Ablation Trial; ODM derived from: https://clinicaltrials.gov/show/NCT01891825

Link

https://clinicaltrials.gov/show/NCT01891825

Keywords

Versions (1)
  1. 8/8/19 8/8/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

August 8, 2019

DOI

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License

Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT01891825

English

Eligibility Atrial Fibrillation NCT01891825

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
symptomatic persistent or long-standing af suitable for af ablation.
Description

Persistent atrial fibrillation Symptomatic | Atrial Fibrillation Long-term | Patient Suitable Catheter ablation for atrial fibrillation

Data type

boolean

Alias
UMLS CUI [1,1]
C2585653
UMLS CUI [1,2]
C0231220
UMLS CUI [2,1]
C0004238
UMLS CUI [2,2]
C0443252
UMLS CUI [3,1]
C0030705
UMLS CUI [3,2]
C3900053
UMLS CUI [3,3]
C2702800
age over 18 years old.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
informed consent to participate in this study.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
pre-existing ilrs or permanent pacemakers that do not allow for continuous monitoring for af occurrence, or are not mri-safe.
Description

implantable loop recorder present | Permanent pacemaker | Atrial fibrillation monitoring Unsuccessful | Difficulty with MRI

Data type

boolean

Alias
UMLS CUI [1]
C3838353
UMLS CUI [2]
C0281945
UMLS CUI [3,1]
C1276351
UMLS CUI [3,2]
C1272705
UMLS CUI [4,1]
C0332218
UMLS CUI [4,2]
C0024485
unable to undergo general anaesthesia for af ablation.
Description

General Anesthesia Unable Atrial Fibrillation

Data type

boolean

Alias
UMLS CUI [1,1]
C0002915
UMLS CUI [1,2]
C1299582
UMLS CUI [1,3]
C0004238
previous cardiac surgery, such as coronary artery bypass grafting or valvular surgery.
Description

Cardiac Surgery Previous | Coronary Artery Bypass Surgery | Operation on heart valve

Data type

boolean

Alias
UMLS CUI [1,1]
C0018821
UMLS CUI [1,2]
C0205156
UMLS CUI [2]
C0010055
UMLS CUI [3]
C0190065
scheduled for elective cardiac surgery, such as coronary artery bypass grafting or valvular surgery.
Description

Cardiac Surgery elective Scheduled | Coronary Artery Bypass Surgery | Operation on heart valve

Data type

boolean

Alias
UMLS CUI [1,1]
C0018821
UMLS CUI [1,2]
C0439608
UMLS CUI [1,3]
C0205539
UMLS CUI [2]
C0010055
UMLS CUI [3]
C0190065
previous thoracic surgery.
Description

Thoracic Surgical Procedure

Data type

boolean

Alias
UMLS CUI [1]
C0524832
participation in a conflicting study.
Description

Study Subject Participation Status Interferes with Clinical Trial

Data type

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0008976
potential participants who are mentally incapacitated and cannot consent or comply with follow-up
Description

Mental handicap | Informed Consent Unable | Compliance Unable Follow-up

Data type

boolean

Alias
UMLS CUI [1]
C1306341
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C1299582
UMLS CUI [3,1]
C1321605
UMLS CUI [3,2]
C1299582
UMLS CUI [3,3]
C3274571
pregnancy
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
other cardiac rhythm disorders
Description

Cardiac Arrhythmia

Data type

boolean

Alias
UMLS CUI [1]
C0003811
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Similar models

Eligibility Atrial Fibrillation NCT01891825

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Persistent atrial fibrillation Symptomatic | Atrial Fibrillation Long-term | Patient Suitable Catheter ablation for atrial fibrillation
Item
symptomatic persistent or long-standing af suitable for af ablation.
boolean
C2585653 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C0004238 (UMLS CUI [2,1])
C0443252 (UMLS CUI [2,2])
C0030705 (UMLS CUI [3,1])
C3900053 (UMLS CUI [3,2])
C2702800 (UMLS CUI [3,3])
Age
Item
age over 18 years old.
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
informed consent to participate in this study.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
implantable loop recorder present | Permanent pacemaker | Atrial fibrillation monitoring Unsuccessful | Difficulty with MRI
Item
pre-existing ilrs or permanent pacemakers that do not allow for continuous monitoring for af occurrence, or are not mri-safe.
boolean
C3838353 (UMLS CUI [1])
C0281945 (UMLS CUI [2])
C1276351 (UMLS CUI [3,1])
C1272705 (UMLS CUI [3,2])
C0332218 (UMLS CUI [4,1])
C0024485 (UMLS CUI [4,2])
General Anesthesia Unable Atrial Fibrillation
Item
unable to undergo general anaesthesia for af ablation.
boolean
C0002915 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0004238 (UMLS CUI [1,3])
Cardiac Surgery Previous | Coronary Artery Bypass Surgery | Operation on heart valve
Item
previous cardiac surgery, such as coronary artery bypass grafting or valvular surgery.
boolean
C0018821 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C0010055 (UMLS CUI [2])
C0190065 (UMLS CUI [3])
Cardiac Surgery elective Scheduled | Coronary Artery Bypass Surgery | Operation on heart valve
Item
scheduled for elective cardiac surgery, such as coronary artery bypass grafting or valvular surgery.
boolean
C0018821 (UMLS CUI [1,1])
C0439608 (UMLS CUI [1,2])
C0205539 (UMLS CUI [1,3])
C0010055 (UMLS CUI [2])
C0190065 (UMLS CUI [3])
Thoracic Surgical Procedure
Item
previous thoracic surgery.
boolean
C0524832 (UMLS CUI [1])
Study Subject Participation Status Interferes with Clinical Trial
Item
participation in a conflicting study.
boolean
C2348568 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
Mental handicap | Informed Consent Unable | Compliance Unable Follow-up
Item
potential participants who are mentally incapacitated and cannot consent or comply with follow-up
boolean
C1306341 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
C1321605 (UMLS CUI [3,1])
C1299582 (UMLS CUI [3,2])
C3274571 (UMLS CUI [3,3])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Cardiac Arrhythmia
Item
other cardiac rhythm disorders
boolean
C0003811 (UMLS CUI [1])
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