ID

37494

Description

Atrial Fibrillation After Catheter Versus Thoracoscopic Ablation Using Patient Activated Implantable Loop Recorders: The ACTUAL Study; ODM derived from: https://clinicaltrials.gov/show/NCT01503268

Lien

https://clinicaltrials.gov/show/NCT01503268

Mots-clés

  1. 02/08/2019 02/08/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

2 août 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Atrial Fibrillation NCT01503268

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])

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