Informações:
Falhas:
ID
37494
Descrição
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
Palavras-chave
Versões (1)
- 02/08/2019 02/08/2019 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
2 de agosto de 2019
DOI
Para um pedido faça login.
Licença
Creative Commons BY 4.0
Comentários do modelo :
Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.
Comentários do grupo de itens para :
Comentários do item para :
Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.
Eligibility Atrial Fibrillation NCT01503268
Eligibility Atrial Fibrillation NCT01503268
- StudyEvent: Eligibility
Similar models
Eligibility Atrial Fibrillation NCT01503268
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Persistent atrial fibrillation Symptomatic
Item
symptomatic persistent atrial fibrillation
boolean
C2585653 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
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])
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])
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])
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])
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])
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])
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])