Actively Recruiting
Registry on Electrophysiological Studies and Electrical Cardioversion at University Hospital Düsseldorf
Led by Heinrich-Heine University, Duesseldorf · Updated on 2025-09-29
1000
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are collecting data on patients undergoing electrophysiological studies (EPS), catheter ablation, and electrical cardioversion at University Hospital Düsseldorf. This observational registry gathers both retrospective data from 2011 and prospective data since 2015 to evaluate the safety, effectiveness, and clinical outcomes of these standard procedures in everyday medical care. The goal is to improve quality assurance and identify factors that affect patient outcomes. The registry includes patients treated with EPS, catheter ablation, or electrical cardioversion. No additional invasive procedures are done for study purposes, and participation does not change routine care decisions. Patients are followed up routinely at 1, 3, 6, 12, and 24 months after the procedure, with possible additional phone interviews to gather more information. Participants provide data on demographics, medical history, lab and imaging results, procedure details, and follow-up outcomes. Researchers focus on safety by tracking complications during and after procedures, as well as effectiveness by monitoring arrhythmia recurrence and need for further treatments. They also record hospitalizations and overall survival for up to 24 months post-procedure to help optimize future patient care.
CONDITIONS
Brief Title
Electrophysiological Registry Duesseldorf
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients who have undergone an electrophysiological study or electrical cardioversion at University Hospital Düsseldorf since 2015 (retrospective cohort)
- Patients scheduled to undergo an electrophysiological study or electrical cardioversion at University Hospital Düsseldorf from 2019 onward (prospective cohort)
- Written informed consent for participation in the registry (prospective part only)
You will not qualify if you...
- Younger than 18 years
- Lack of written informed consent
- Pregnancy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Procedure day
Participants undergo electrophysiological studies, catheter ablation, or electrical cardioversion as part of routine care.
1 visit (in-person)
Duration - Up to 24 months
Participants are followed to monitor safety and clinical outcomes after their procedure.
Follow-up visits at 1, 3, 6, 12, and 24 months, with additional telephone interviews as needed
Trial Site Locations
Total: 1 location
1
University Hospital Duesseldorf
Düsseldorf, Germany, 40225
Actively Recruiting
Research Team
O
Obaida Rana, MD
L
Lisa Dannenberg, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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