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NCT04906668Active, not recruiting

ABLATE Versus PACE: PVI or AV Node Ablation and PM Implantation for Elderly Patients With Persistent AF

Pulmonary-vein Isolation or Ablation of Atrioventricular-node and Pacemaker Implantation for Elderly Patients With Persistent Atrial Fibrillation (ABLATE Versus PACE)

Source: ClinicalTrials.gov · Last updated 17 Sept 2025

Brief summary (registry, in English)

As patients age, symptom control and treatment of atrial fibrillation become equally difficult, often leading to increased hospitalization. ABLATE versus PACE is a prospective, randomized clinical trial comparing pacemaker implantation with AV node ablation with pulmonary vein isolation in terms of rehospitalization and quality of life in patients with persistent AF aged 75 years and older.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
196 (estimated)
First submitted
19 May 2021
Start date
1 May 2021
Primary completion date
30 May 2026
Lead sponsor
St. Josefs-Hospital Wiesbaden GmbH
NCT number
NCT04906668

What you commit to

  • Study type: Interventional
  • Planned participants: 196
  • From 1 May 2021 to the primary completion date, 30 May 2026
  • 12 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Surgical coronary revascularization (within the last 90 days) or current triple therapy after stent PCI
  • concomitant participation in another registered trial

Other illness

  • High-grade (III°) left cardiac valvular disease

Lab values

  • impaired systolic left ventricular function (ejection fraction \< 50%)

Other

  • pre-implanted pacemaker
  • bradycardia-indication for pacemaker
  • contraindication for PVI or pacemaker-implantation
  • contraindication for oral anticoagulation
  • body-mass-index BMI \> 40 kg/m2
  • inability to give written informed consent
  • life expectancy \< 12 months
  • reversible cause of AF (e.g. thyrotoxicosis, alcohol ingestion)

Who the study is looking for

  • Persistent AF according to current ESC guideline (2020)
  • Symptoms EHRA classification II - IV despite guideline indicated medical therapy
  • Age ≥ 75 years
  • Capability of giving written informed consent

Age in the registry: 75 years to 99 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (12)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Universitätsklinikum Innsbruck
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InnsbruckAustriaUnknown status
Kerckhoff Klinik, Bad Nauheim
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Bad NauheimGermanyUnknown status
Vivantes Klinikum am Urban
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BerlinGermanyUnknown status
Universitätsklinikum Essen
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EssenGermanyUnknown status
Universitätsklinikum Frankfurt am Main
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FrankfurtGermanyUnknown status
Klinikum Fürth
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FürthGermanyUnknown status
Ev. Krankenhaus Hagen-Haspe
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HagenGermanyUnknown status
Asklepios Klinik St. Georg
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HamburgGermanyUnknown status
Westpfalz-Klinikum - Kaiserslautern
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KaiserslauternGermanyUnknown status
Krankenhaus Landshut-Achdorf
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LandshutGermanyUnknown status
Universitätsklinikum Münster
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MünsterGermanyUnknown status
St. Josefs-Hospital Wiesbaden GmbH
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WiesbadenGermanyUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.