Registry of heart rhythm procedures at University Hospital Düsseldorf
Collects data on heart rhythm tests and treatments in patients with irregular heartbeat.
Plain-language title generated from the registry record
Registry title: Electrophysiological Registry Duesseldorf
Key facts
- Where
- Düsseldorf, GermanySee the site
Where in Germany
- University Hospital DuesseldorfDüsseldorf, GermanyTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Heinrich-Heine University, Duesseldorf
- Trial code
- NCT07196176
- Record updated
- 29 September 2025
- Original description
This registry at University Hospital Düsseldorf collects retrospective and prospective (from 2019 onward) data on patients undergoing electrophysiological studies (EPS), catheter ablation, and electrical cardioversion. The primary goal is to evaluate safety, efficacy, and clinical outcomes of these standard procedures in routine care. Data will be used for quality assurance and to identify prognostic patient- and procedure-related factors.Read full original descriptionShow less
Registry on Electrophysiological Studies (EPS) at University Hospital Düsseldorf
This registry at University Hospital Düsseldorf collects retrospective and prospective (from 2019 onward) data on patients undergoing electrophysiological studies (EPS), catheter ablation, and electrical cardioversion. The primary goal is to evaluate safety, efficacy, and clinical outcomes of these standard procedures in routine care. Data will be used for quality assurance and to identify prognostic patient- and procedure-related factors.
Inclusion: Patients who undergo an electrophysiological study (EPS) or electrical cardioversion at University Hospital Düsseldorf since 2015 (retrospective cohort); Patients scheduled to undergo an EPS or electrical cardioversion at University Hospital Düsseldorf from 2019 onward (prospective cohort) •- Written informed consent for participation in the registry (prospective part only).
Exclusion: < 18 years; Lack of written informed consent; Pregnancy.