Actively Recruiting

Age: 18Years +
All Genders
ID06977139

Interventional Structural Registry - LuEbeck

Led by Prof. Dr. med. Ingo Eitel · Updated on 2025-05-18

2000

Participants Needed

1

Research Sites

260 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating the effects of catheter-assisted procedures on patients with structural heart disease. This observational registry aims to understand the impact of these procedures on clinical outcomes such as morbidity and mortality. The study also focuses on evaluating safety and effectiveness in both short-term and long-term periods after the procedures, as well as examining underlying and accompanying health conditions and therapies. Participants in this registry have undergone catheter-based interventions for structural heart disease. The study collects data on various factors including the methods used for treatment, the safety of the procedures during and after intervention, and the effectiveness over hospital stays and extended follow-up. There is no experimental treatment given, as this is an observational study documenting real-world patient outcomes. During the study, researchers will monitor participants' health and review combined clinical events occurring within 30 days after the catheter procedures. Data collection includes evaluating patient conditions, concomitant diseases, safety outcomes, and treatment effectiveness over time. The observation period is long-term, allowing for ongoing assessment of patient prognosis following catheter-based treatment. Participation involves providing consent and sharing medical information relevant to the registry objectives.

CONDITIONS

Brief Title

Interventional Structural Registry - LuEbeck

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Structural heart disease
  • Age 18 years or older
  • Ability to provide consent and information
Not Eligible

You will not qualify if you...

  • Patients without consent or information
  • Age 18 years or younger

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to 10 years

Participants with structural heart disease are observed over time to collect health data related to their condition.

Periodic visits as needed for data collection

Trial Site Locations

Total: 1 location

1

Universitätsklinikum Schleswig-Holstein

Lübeck, Schleswig-Holstein, Germany

Actively Recruiting

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Research Team

I

Ingo Eitel, Prof. Dr.

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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