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German Ablation Quality-Register

NCT ID: NCT01197638

Last Updated: 2016-06-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

20663 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-06-30

Study Completion Date

2016-02-29

Brief Summary

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The goal of this register is the documentation of the success as well as of the complications regarding interventional therapy of cardiac arrhythmia by catheter ablation. This is the necessary basis for quality management and development of possible improvements of catheter ablation.

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Detailed Description

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The interventional therapy of heartbeat disturbances by means of catheter ablation makes the curative treatment possible of numerous tachycardiac arrhythmics. By this crucial improvement of the supply of patients and its quality of life a genuine healing of a multiplicity of heartbeat disturbances became possible. Especially within the range of the ablation treatment there are relatively few con-trolled studies, which would give a broad collection of the results of the catheter ablation in the different indication areas.

Aim of the registry:

Documentation of indication, hospital course and complications during long term follow-up of patients with catheter ablation

Design:

Prospective, multicenter registry; FU-duration 12 months.

Duration:

Phase I: 2 years

Inclusion criteria:

Catheter ablation (intention to treat)

Exclusion criteria:

Missing declaration of consent

Conditions

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Arrhythmia

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* The ablation register will include all consecutive patients with a performed or attempted electrophysiological ablation

Exclusion Criteria

* Missing signed informed consent
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Stiftung Institut fuer Herzinfarktforschung

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Jochen Senges, MD

Role: PRINCIPAL_INVESTIGATOR

Stiftung Institut fuer Herzinfarktforschung

Locations

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Herz- und Gefäßklinik

Bad Neustadt / Saale, , Germany

Site Status

Vivantes Klinikum Am Urban

Berlin, , Germany

Site Status

St. Marien Hospital

Bonn, , Germany

Site Status

Klinikum Coburg

Coburg, , Germany

Site Status

Praxisklinik Herz und Gefäß,

Dresden, , Germany

Site Status

Asklepios Klinik St Georg

Hamburg, , Germany

Site Status

Universitäres Herzzentrum Hamburg

Hamburg, , Germany

Site Status

Städt Klinikum Hildesheim

Hildesheim, , Germany

Site Status

Krankenhaus München Bogenhausen

München, , Germany

Site Status

Countries

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Germany

References

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Schleberger R, Metzner A, Kuck KH, Andresen D, Willems S, Hoffmann E, Deneke T, Eckardt L, Brachmann J, Hochadel M, Senges J, Rillig A. Antiarrhythmic drug therapy after catheter ablation for atrial fibrillation-Insights from the German Ablation Registry. Pharmacol Res Perspect. 2021 Dec;9(6):e00880. doi: 10.1002/prp2.880.

Reference Type DERIVED
PMID: 34664789 (View on PubMed)

Dechering DG, Gonska BD, Brachmann J, Lewalter T, Kuck KH, Andresen D, Willems S, Spitzer SG, Straube F, Schumacher B, Hochadel M, Senges J, Eckardt L. Efficacy and complications of cavo-tricuspid isthmus-dependent atrial flutter ablation in patients with and without structural heart disease: results from the German Ablation Registry. J Interv Card Electrophysiol. 2021 Jun;61(1):55-62. doi: 10.1007/s10840-020-00769-z. Epub 2020 May 27.

Reference Type DERIVED
PMID: 32458180 (View on PubMed)

Other Identifiers

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Ablations Register

Identifier Type: -

Identifier Source: org_study_id

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