Skip to content

German Ablation Quality-Register

Deutsches Ablations-Qualitätsregister

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01197638
Enrollment
20663
Registered
2010-09-09
Start date
2008-06-30
Completion date
2016-02-29
Last updated
2016-06-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arrhythmia

Keywords

Cardiac arrhythmia, Catheter ablation, Register

Brief summary

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.

Detailed description

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

Interventions

None listed

Sponsors

Stiftung Institut fuer Herzinfarktforschung
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

* Missing signed informed consent

Design outcomes

Primary

MeasureTime frame
Characterize consecutive patients with electrophysiological ablation in daily hospital routine in Germany.01/06/2008-12/31/2011

Secondary

MeasureTime frame
Documentation of further necessary interventions after the initial ablation during hospital stay01/06/2008-12/31/2011
Documentation of hospital mortality, serious but non-fatal complications (stroke, TIA, myocardial infarction, resuscitation), and complications caused by bleedings (serious as well as moderate)01/06/2008-12/31/2011
Documentation of medication therapy at hospital discharge01/06/2008-12/31/2011
Documentation of the 1-year mortality, serious but non-fatal complications (stroke, TIA, myocardial infarction, resuscitation), of heavy bleedings, of phrenicus pareses, PV-stenoses, or fistulas01/06/2008-12/31/2011
Documentation of the technical implementation of ablation and the success of the intervention01/06/2008-12/31/2011
Documentation of needed interventions (implantation of either pacemaker, ICD or CRT, revascularization, a further ablation) during the first year after ablation01/06/2008-12/31/2011
Documentation of hospitalizations during the first year after ablation01/06/2008-12/31/2011
Documentation of medication therapy after 12 months01/06/2008-12/31/2011
Documentation of the absence of relapse and of symptomatology after one year01/06/2008-12/31/2011

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026