ID

37494

Beschrijving

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

Link

https://clinicaltrials.gov/show/NCT01503268

Trefwoorden

  1. 02-08-19 02-08-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

2 augustus 2019

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0

Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Atrial Fibrillation NCT01503268

Eligibility Atrial Fibrillation NCT01503268

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
symptomatic persistent atrial fibrillation
Beschrijving

Persistent atrial fibrillation Symptomatic

Datatype

boolean

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

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
informed consent
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

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.
Beschrijving

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

Datatype

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.
Beschrijving

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

Datatype

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
Beschrijving

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

Datatype

boolean

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

Thoracic Surgical Procedure

Datatype

boolean

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

Study Subject Participation Status Interferes with Clinical Trial

Datatype

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
Beschrijving

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

Datatype

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
Beschrijving

Pregnancy

Datatype

boolean

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

Cardiac Arrhythmia

Datatype

boolean

Alias
UMLS CUI [1]
C0003811

Similar models

Eligibility Atrial Fibrillation NCT01503268

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial