Informazione:
Errore:
ID
14650
Descrizione
Impedance vs. Contact Force Guided Atrial Fibrillation Ablation Using Automated Annotation System; ODM derived from: https://clinicaltrials.gov/show/NCT02364401
collegamento
https://clinicaltrials.gov/show/NCT02364401
Keywords
versioni (1)
- 25/04/16 25/04/16 -
Caricato su
25 aprile 2016
DOI
Per favore, per richiedere un accesso.
Licenza
Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT02364401
Eligibility Atrial Fibrillation NCT02364401
- StudyEvent: Eligibility
Similar models
Eligibility Atrial Fibrillation NCT02364401
- StudyEvent: Eligibility
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Atrial Fibrillation | Heart Valves
Item
patients with non-valvular atrial fibrillation
boolean
C0004238 (UMLS CUI [1])
C0018826 (UMLS CUI [2])
C0018826 (UMLS CUI [2])
Atrial Fibrillation | Therapeutic procedure Anti-Arrhythmia Agents
Item
patients having atrial fibrillation even after receiving continued treatment with at least 1 antiarrhythmic drug for more than 6 weeks
boolean
C0004238 (UMLS CUI [1])
C0087111 (UMLS CUI [2,1])
C0003195 (UMLS CUI [2,2])
C0087111 (UMLS CUI [2,1])
C0003195 (UMLS CUI [2,2])
Bradycardia-tachycardia syndrome | Atrial Fibrillation
Item
patients with tachycardia-bradycardia syndrome associated with atrial fibrillation.
boolean
C0221047 (UMLS CUI [1])
C0004238 (UMLS CUI [2])
C0004238 (UMLS CUI [2])
Comprehension Informed Consent Cardiac ablation
Item
patients who can understand the information sheet and consent form on the need and procedure of catheter ablation and submitted them
boolean
C0162340 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C0162563 (UMLS CUI [1,3])
C0021430 (UMLS CUI [1,2])
C0162563 (UMLS CUI [1,3])
Availability of follow-up | Cardiac ablation
Item
patients who are available of follow-up at least for more than three months after catheter ablation
boolean
C0470187 (UMLS CUI [1,1])
C1522577 (UMLS CUI [1,2])
C0162563 (UMLS CUI [2])
C1522577 (UMLS CUI [1,2])
C0162563 (UMLS CUI [2])
Inappropriate Cardiac ablation | Left atrial structure Size
Item
patients unsuitable for catheter ablation because the size of left atrium is over 5.5cm
boolean
C1548788 (UMLS CUI [1,1])
C0162563 (UMLS CUI [1,2])
C0225860 (UMLS CUI [2,1])
C0456389 (UMLS CUI [2,2])
C0162563 (UMLS CUI [1,2])
C0225860 (UMLS CUI [2,1])
C0456389 (UMLS CUI [2,2])
Inappropriate Cardiac ablation | Pulmonary Surgical Procedures | Structural disorder of heart
Item
patients unsuitable for catheter ablation due to previous history of pulmonary surgery or structural heat disease.
boolean
C1548788 (UMLS CUI [1,1])
C0162563 (UMLS CUI [1,2])
C0038903 (UMLS CUI [2])
C1290384 (UMLS CUI [3])
C0162563 (UMLS CUI [1,2])
C0038903 (UMLS CUI [2])
C1290384 (UMLS CUI [3])
Unable Anticoagulation Therapy | Catheter Ablation, Radiofrequency
Item
patients who cannot receive standard treatments such as anticoagulation therapy which need to be continuously performed prior to radiofrequency catheter ablation
boolean
C1299582 (UMLS CUI [1,1])
C0003281 (UMLS CUI [1,2])
C0162561 (UMLS CUI [2])
C0003281 (UMLS CUI [1,2])
C0162561 (UMLS CUI [2])
Vulnerable adult Clinical Research
Item
patients in the subject group vulnerable to clinical study
boolean
C1562367 (UMLS CUI [1,1])
C0008972 (UMLS CUI [1,2])
C0008972 (UMLS CUI [1,2])
Previous Cardiac ablation Atrial Fibrillation
Item
patients who had undergone a prior catheter ablation for atrial fibrillation
boolean
C0205156 (UMLS CUI [1,1])
C0162563 (UMLS CUI [1,2])
C0004238 (UMLS CUI [1,3])
C0162563 (UMLS CUI [1,2])
C0004238 (UMLS CUI [1,3])