Informatie:
Fout:
ID
34067
Beschrijving
Atrial Fibrillation Force Contact Ablation Study; ODM derived from: https://clinicaltrials.gov/show/NCT01693107
Link
https://clinicaltrials.gov/show/NCT01693107
Trefwoorden
Versies (1)
- 14-01-19 14-01-19 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
14 januari 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 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)
Datatype
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])