CClinicalTrials.gg
Status unknownNCT04753541AF GENUpdated Feb 15, 2021

The Influence of Genetic Predisposition on Outcome After Catheter Ablation of Atrial Fibrillation.

An observational study in Atrial Fibrillation, sponsored by Deutsches Herzzentrum Muenchen. Status unknown at 1 site in Germany. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2021-02-15.

Sponsored by Deutsches Herzzentrum Muenchen · Observational

The sponsor has not verified this record recently (last verified Feb 2021), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
1,000
Ages
18 Years and older
Sex
All
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Study summary

Catheter ablation is an established standard therapy in interventional treatment of atrial fibrillation.The trial investigates the influence of genetic risk for the recurrence of atrial fibrillation after catheter ablation.

Read the detailed description

Catheter ablation is an established standard therapy in interventional treatment of atrial fibrillation. electric isolation of the pulmonary veins, from which atrial fibrillation is originating in most patients, is cornerstone of all atrial fibrillation patients.

The most common cause for AF recurrence is still incomplete isolation of the pulmonary veins, on the other hand, only 80% of paroxysmal and 60 % of persistent patients can successfully be cured from atrial fibrillation (despite of isolated pulmonary veins after multiple ablation procedures).

By now, non-procedure related predictive risk factors, resulting in recurrence of atrial fibrillation after catheter ablation, are only partially identified, such as obesity, hypertension and sleep apnea.

In the past year several genetic risk alleles were identified, which are associated with atrial fibrillation. By now the relation between genetic risk, which is determined for every patient by its specific genotype and the outcome of catheter ablation in paroxysmal and persistent atrial fibrillation has not yet been investigated.

The aim is to investigate the influence of genetic risk for the recurrence of atrial fibrillation after catheter ablation.

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Conditions studied

  • Atrial Fibrillation

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03

In context

Atrial Fibrillation

3,870 studies on the registry are indexed under Atrial Fibrillation; 924 are open to participants now.

This study's planned enrollment of 1,000 is above the median of 300 across 1,363 observational studies indexed under Atrial Fibrillation.

Browse Atrial Fibrillation studies →

Lead sponsor

Deutsches Herzzentrum Muenchen is the lead sponsor of 112 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

patients planned for primary ablation due to paroxysmale or persistent atrial fibrillation

Inclusion criteria

  • patients planned for primary ablation due to paroxysmale or persistent atrial fibrillation
  • written informed consent

Exclusion criteria

Exclusion Criteria:

  • patients under 18 years of age or patients not able to give informed consent
  • prior left atrial ablation
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
1,000 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Interventions

  • Otherno intervention

    this is not an interventional study

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What researchers measure

Primary outcomes

  1. Influence of genetic risk on atrial fibrillation

    Analysation of the influence of genetic risk on the probability of recurrence of atrial fibrillation after catheter ablation

    Time frame: 10ml blood sample taken at baseline visit (routine blood sample)

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Study locations

1 of 1 sites recruiting
  • Deutsches Herzzentrum Muenchen
    Munich, 80636, Germany
    • Isabel Deisenhofer, MD · Contact · deisenhofer@dhm.mhn.de · +49 89 1218 2020
    • Isabel Deisenhofer, MD · Sub investigator
    Recruiting
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 15, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04753541
Lead sponsor
Deutsches Herzzentrum Muenchen
Responsible party
Sponsor
First posted
Feb 15, 2021
Start date
Nov 1, 2020
Primary completion
Jun 2023 (estimated)
Completion
Jun 2023 (estimated)
Last update
Feb 15, 2021

Study contacts

Felix Bourier, MD
Contact
bourier@dhm.mhn.de
+49891218 ext. 2020
Heike Starkmann
Contact
starkmannh@dhm.mhn.de
+49891218 ext. 1192
Bourier Felix, MD
principal investigator · Deutsches Herzzentrum München

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Feb 2021. You cannot join it, but the record below documents what was studied.

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