Actively Recruiting

Age: 18Years +
All Genders
ID07196176

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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)
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - Procedure day

Participants undergo electrophysiological studies, catheter ablation, or electrical cardioversion as part of routine care.

1 visit (in-person)

Long-term Monitoring

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

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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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