Informations:
Erreur:
ID
34067
Description
Atrial Fibrillation Force Contact Ablation Study; ODM derived from: https://clinicaltrials.gov/show/NCT01693107
Lien
https://clinicaltrials.gov/show/NCT01693107
Mots-clés
Versions (1)
- 14/01/2019 14/01/2019 -
Détendeur de droits
See clinicaltrials.gov
Téléchargé le
14 janvier 2019
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
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Eligibility Paroxysmal Atrial Fibrillation NCT01693107
Eligibility Paroxysmal Atrial Fibrillation NCT01693107
- StudyEvent: Eligibility
Similar models
Eligibility Paroxysmal Atrial Fibrillation NCT01693107
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Age
Item
patients aged 18 years or greater.
boolean
C0001779 (UMLS CUI [1])
Pulmonary vein Catheter ablation for atrial fibrillation Firstly
Item
patients undergoing first-time pulmonary vein catheter ablation for af.
boolean
C0034090 (UMLS CUI [1,1])
C2702800 (UMLS CUI [1,2])
C1279901 (UMLS CUI [1,3])
C2702800 (UMLS CUI [1,2])
C1279901 (UMLS CUI [1,3])
Paroxysmal atrial fibrillation | Atrial Fibrillation Episodes Symptomatic Duration | Cardioversion Atrial Fibrillation Episodes Symptomatic
Item
patients with paroxysmal af. paroxysmal af will be defined as symptomatic episodes of af lasting less than 7 days or treated with cardioversion(s) within 48 hours of onset.
boolean
C0235480 (UMLS CUI [1])
C0004238 (UMLS CUI [2,1])
C0332189 (UMLS CUI [2,2])
C0231220 (UMLS CUI [2,3])
C0449238 (UMLS CUI [2,4])
C0013778 (UMLS CUI [3,1])
C0004238 (UMLS CUI [3,2])
C0332189 (UMLS CUI [3,3])
C0231220 (UMLS CUI [3,4])
C0004238 (UMLS CUI [2,1])
C0332189 (UMLS CUI [2,2])
C0231220 (UMLS CUI [2,3])
C0449238 (UMLS CUI [2,4])
C0013778 (UMLS CUI [3,1])
C0004238 (UMLS CUI [3,2])
C0332189 (UMLS CUI [3,3])
C0231220 (UMLS CUI [3,4])
Atrial Fibrillation Episode Quantity | Telemetry | Monitoring, Ambulatory | 12 lead ECG
Item
at least one episode of af must have been documented on telemetry, ambulatory monitor, or 12-lead ecg.
boolean
C0004238 (UMLS CUI [1,1])
C0332189 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0039451 (UMLS CUI [2])
C0242882 (UMLS CUI [3])
C0430456 (UMLS CUI [4])
C0332189 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0039451 (UMLS CUI [2])
C0242882 (UMLS CUI [3])
C0430456 (UMLS CUI [4])
Informed Consent
Item
patients must be able and willing to provide written informed consent to participate in the clinical study.
boolean
C0021430 (UMLS CUI [1])
Ablation Atrial Fibrillation
Item
patients with a history of any previous ablation for atrial fibrillation.
boolean
C0547070 (UMLS CUI [1,1])
C0004238 (UMLS CUI [1,2])
C0004238 (UMLS CUI [1,2])
Atriotomy Scar | Replacement of mitral valve | Replacement of tricuspid valve | Mitral valvuloplasty | Repair of tricuspid valve | ASD Surgery | Heart Transplantation
Item
patients with a previous atriotomy scar, ie. mitral or tricuspid valve replacement or repair, asd surgery, cardiac transplant.
boolean
C0189760 (UMLS CUI [1,1])
C0241158 (UMLS CUI [1,2])
C0026268 (UMLS CUI [2])
C0190119 (UMLS CUI [3])
C0396849 (UMLS CUI [4])
C0396899 (UMLS CUI [5])
C0018817 (UMLS CUI [6,1])
C0543467 (UMLS CUI [6,2])
C0018823 (UMLS CUI [7])
C0241158 (UMLS CUI [1,2])
C0026268 (UMLS CUI [2])
C0190119 (UMLS CUI [3])
C0396849 (UMLS CUI [4])
C0396899 (UMLS CUI [5])
C0018817 (UMLS CUI [6,1])
C0543467 (UMLS CUI [6,2])
C0018823 (UMLS CUI [7])
Intracardiac thrombus
Item
patients with an intracardiac thrombus
boolean
C0876998 (UMLS CUI [1])
Pregnancy | Possible pregnancy
Item
patients who are or may potentially be pregnant.
boolean
C0032961 (UMLS CUI [1])
C0425965 (UMLS CUI [2])
C0425965 (UMLS CUI [2])