ConTempoRary Cardiac Stimulation in Clinical practicE: lEft, BivEntriculAr, Right, and conDuction System Pacing
Recruiting
Observational Study
Arrhythmias, Cardiac
Atrioventricular Block
Reduced Systolic Function
Atrial Fibrillation
Bradyarrhythmia
Ventricular Tachycardia
Ventricular Dysfunction
Ventricular Fibrillation
Ventricular Arrythmia
Atrioventricular Nodal Disease
Atrioventricular Conduction Defects
Atrioventricular Block Complete
Atrioventricular Block Incomplete
Atrioventricular Junctional Rhythm
Bundle-Branch Block
Left Bundle-Branch Block
Heart Failure, Systolic
Block;Atrioventricular
Block; Arrhythmic
Block; Mobitz
Block, Heart
Block, Fascicular
Block Branch Bundle Left
Heart Failure，Congestive
Heart Arrhythmia
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 8,400 (estimated)
- Sponsor
- University Hospital of Ferrara · Other
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About This Trial
The goal of this observational study is to evaluate the clinical characteristics of patients undergoing permanent cardiac pacing and to compare procedural efficacy and safety of different implantation approaches in the clinical practice of the participating centres. The contribution of non-fluoroscopic anatomical and electrophysiological reconstruction systems to device implantation procedures wil…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Indication for cardiac stimulation
* Having performed the implantation of a device for cardiac stimulation
Exclusion Criteria:
* Age \< 18 years;
* Pregnancy status;
Contacts