CAT-PVC: Catheter Ablation Versus Amiodarone for Therapy of Premature Ventricular Contractions in Patients With Structural Heart Disease

Sponsor
University of Leipzig (Other)
Overall Status
Completed
CT.gov ID
NCT02924285
Collaborator
Leipzig Heart Institute GmbH (Other), Abbott Medical Devices (Industry), Zentrum für Klinische Studien Leipzig (Other)
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Study Details

Study Description

Brief Summary

For therapy of symptomatic premature ventricular complexes (PVCs) in subjects with structural heart disease the current European Guidelines for the management of patients with ventricular arrhythmias and the prevention of second cardiac death recommend catheter ablation as well as amiodarone with a class IIa indication. Due to the lack of randomized data this study investigates the comparison of catheter ablation and amiodarone for PVC treatment in patients with structural heart disease. Therefore, patients will be randomized to one of two treatment strategies: 1) catheter ablation, or 2) amiodarone.

Condition or Disease Intervention/Treatment Phase
Phase 3

Detailed Description

Premature ventricular contractions (PVCs) are frequently encountered in patients with or without structural heart disease. Even though PVCs in healthy subjects are considered to be a benign arrhythmia. There is also evidence for the risk of a reversible cardiomyopathy due to the PVC-induced inter- and intraventricular dyssynchrony. Data show that elimination of PVCs by catheter ablation leads to an improvement of left ventricular dysfunction. In one-half of the heart failure patients frequent PVCs occur with more than 1000/24 h. In patients with structural heart disease premature ventricular contractions (PVCs) lead to an increased mortality risk with only a burden of 10 PVC per hour. Further decreasing of left ventricular function and worsening of heart failure are described. Therefore, therapy of frequent monomorphic PVCs is recommended in these subjects. Beta-blockers as part of standard therapy often remain ineffective or may lead to a paradoxic effect in patients with bradycardia. A limiting factor for selection of antiarrhythmic drug due to increasing mortality is the presence of structural heart disease. So in the most cases amiodarone is indicated. There are data showing improvement of LV function after suppression of PVCs by amiodarone with a significant reduction of the PVC burden in comparison to baseline. However, the adverse effects of amiodarone are well-known especially in long-term therapy. On the other hand, radiofrequency catheter ablation is a widely applied and safe treatment option for PVCs with a high acute success rate of up to 90% PVC reduction in various circumstances like pre-existing heart failure and post myocardial infarction subjects. Some small-sample studies show the benefit of catheter ablation in subjects with depressed LV function. To date, there are no randomized data for comparison of catheter ablation and amiodarone for therapy of PVCs in patients with structural heart disease.

Study Design

Study Type:
Interventional
Actual Enrollment :
80 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
CAT-PVC Trial Catheter Ablation Versus Amiodarone for Therapy of Premature Ventricular Contractions in Patients With Structural Heart Disease: a Randomized Trial
Actual Study Start Date :
Nov 1, 2017
Actual Primary Completion Date :
Dec 30, 2020
Actual Study Completion Date :
Mar 4, 2021

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Procedure

Radiofrequency catheter ablation

Procedure: Procedure (Radiofrequency catheter ablation)
Radiofrequency catheter ablation

Active Comparator: Antiarrhythmic Drug

Amiodarone

Drug: Amiodarone
Amiodarone, Verification of superiority of catheter ablation over amiodarone for treatment of PVCs in patients with structural heart disease as: Antiarrhythmic Drug Amiodarone

Outcome Measures

Primary Outcome Measures

  1. Verification of superiority of catheter ablation over amiodarone for treatment of PVCs in patients with structural heart disease [Baseline and after 6 weeks]

    difference of the PVC burden in a 24 h Holter registration after 6 weeks and at baseline expressed as the amount of the baseline value ΔVES_r = (VES_6 - VES_0) / VES_0

Secondary Outcome Measures

  1. Change in quality of life (QoL) score according EQ-5D questionnaire [Baseline, after 6 weeks and 12 months]

  2. Change in 6 minute walking distance [Baseline, after 6 weeks and 12 months]

  3. Change in left ventricular ejection fraction (LVEF) [Baseline, after 6 weeks and 12 months]

  4. Change in serum NT-proBNP level [Baseline, after 6 weeks and 12 months]

  5. Change in New York Heart Association (NYHA) functional class [Baseline, after 6 weeks and 12 months]

  6. Occurrence of cardiovascular related hospitalization [after 6 weeks and 12 months]

  7. Occurrence of drug adverse effects [after 6 weeks and 12 months]

  8. Occurrence of procedure related complications [after 6 weeks and 12 months]

  9. Difference of the PVC burden in a 24 h Holter registration after 12 months and at baseline expressed as the amount of the baseline value [Baseline and after 12 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 87 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Structural heart disease with or without left ventricular dysfunction with

  • PVCs on Holter monitoring (burden >10.000/d) AND/OR

  • PVCs on Holter monitoring correlating with symptoms AND/OR

  • Reduction of biventricular pacing <92% in subjects with implanted cardiac resynchronization therapy (CRT) device

  • Age: 18-87 years

  • Willing and capable of giving informed consent

Exclusion Criteria:
  • Previous ablation procedure or amiodarone for PVC without success

  • New York Heart Association (NYHA) functional class IV

  • Intracardial thrombus

  • Pulmonary fibrosis

  • Liver cirrhosis ≥ CHILD B

  • Manifest hyper- or hypothyreoidism

  • Long QT (QTc > 500 ms if QRS<120 ms, if QRS>120 ms according to QTRR, QRS formula)

  • Sick sinus syndrome with symptomatic bradycardia <55 bpm or AV node conduction delay without implanted pacing device

  • Known side effects under amiodarone or iodine

  • Idiopathic angioedema

  • Comedication with known risk for torsade-de-pointes tachycardia

  • Pregnancy or lactation

Contacts and Locations

Locations

Site City State Country Postal Code
1 Heart Center Leipzig Leipzig Germany

Sponsors and Collaborators

  • University of Leipzig
  • Leipzig Heart Institute GmbH
  • Abbott Medical Devices
  • Zentrum für Klinische Studien Leipzig

Investigators

  • Principal Investigator: Gerhard Hindricks, MD, Heart Center Leipzig

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Leipzig
ClinicalTrials.gov Identifier:
NCT02924285
Other Study ID Numbers:
  • CAT-PVC01
First Posted:
Oct 5, 2016
Last Update Posted:
Jul 22, 2021
Last Verified:
Jul 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 22, 2021