Eligibility Atrial Fibrillation NCT01503268

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
symptomatic persistent atrial fibrillation
Description

Persistent atrial fibrillation Symptomatic

Type de données

boolean

Alias
UMLS CUI [1,1]
C2585653
UMLS CUI [1,2]
C0231220
age over 18 years
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
informed consent
Description

Informed Consent

Type de données

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 Pre-existing Preventing Atrial fibrillation monitoring | Permanent pacemaker Preventing Atrial fibrillation monitoring | MRI Unsafe

Type de données

boolean

Alias
UMLS CUI [1,1]
C3838353
UMLS CUI [1,2]
C2347662
UMLS CUI [1,3]
C1292733
UMLS CUI [1,4]
C1276351
UMLS CUI [2,1]
C0281945
UMLS CUI [2,2]
C1292733
UMLS CUI [2,3]
C1276351
UMLS CUI [3,1]
C0024485
UMLS CUI [3,2]
C4036038
patients unable to undergo general anaesthesia for af ablation.
Description

General Anesthesia Receive Unable | General Anesthesia Catheter ablation for atrial fibrillation

Type de données

boolean

Alias
UMLS CUI [1,1]
C0002915
UMLS CUI [1,2]
C1514756
UMLS CUI [1,3]
C1299582
UMLS CUI [2,1]
C0002915
UMLS CUI [2,2]
C2702800
previous cardiac surgery, such as coronary artery bypass grafting or valvular surgery
Description

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

Type de données

boolean

Alias
UMLS CUI [1]
C0018821
UMLS CUI [2]
C0010055
UMLS CUI [3]
C0190065
previous thoracic surgery
Description

Thoracic Surgical Procedure

Type de données

boolean

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

Study Subject Participation Status Interferes with Clinical Trial

Type de données

boolean

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

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

Type de données

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

Type de données

boolean

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

Cardiac Arrhythmia

Type de données

boolean

Alias
UMLS CUI [1]
C0003811

Similar models

Eligibility Atrial Fibrillation NCT01503268

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Persistent atrial fibrillation Symptomatic
Item
symptomatic persistent atrial fibrillation
boolean
C2585653 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
Age
Item
age over 18 years
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
implantable loop recorder Pre-existing Preventing Atrial fibrillation monitoring | Permanent pacemaker Preventing Atrial fibrillation monitoring | MRI Unsafe
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 [1,1])
C2347662 (UMLS CUI [1,2])
C1292733 (UMLS CUI [1,3])
C1276351 (UMLS CUI [1,4])
C0281945 (UMLS CUI [2,1])
C1292733 (UMLS CUI [2,2])
C1276351 (UMLS CUI [2,3])
C0024485 (UMLS CUI [3,1])
C4036038 (UMLS CUI [3,2])
General Anesthesia Receive Unable | General Anesthesia Catheter ablation for atrial fibrillation
Item
patients unable to undergo general anaesthesia for af ablation.
boolean
C0002915 (UMLS CUI [1,1])
C1514756 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C0002915 (UMLS CUI [2,1])
C2702800 (UMLS CUI [2,2])
Cardiac Surgery procedures | 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])
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
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])