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NCT Number: NCT05029570

Heart Rate Regularization in Atrial Fibrilation and Heart Failure

The PACE-FIB trial is a multicentre, randomised, open-label clinical trial. Patients older than 18 years, with permanent AF, LVEF>40%, average resting heart rate ≤ 110 beats per minute (bpm), at least one hospitalisation due to HF in the previous year and basal NT-proBNP level>900 pg/ml will be randomised to either CSP and subsequent AV node ablation (intervention group) vs. pharmacologic rate control optimised according to clinical practice guidelines. The impact of both strategies on a composite primary endpoint of all-cause mortality, HF hospitalisation and worsening HF will be evaluated during a 36-month follow-up.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hospital Universitario 12 de Octubre

Madrid, 28041, Spain

Location status: Recruiting

Location contact

Daniel Rodríguez Muñoz, MD, PhD

CONTACT

[email protected]

+34 917792742

About this study

Permanent atrial fibrillation (AF) causes beat-to-beat heart rate irregularity, which has shown to decrease cardiac output. Observational data suggest that heart rate regularization through atrioventricular (AV) node ablation and pacemaker implantation improves outcomes in heart failure (HF) patients. However, no trials have been conducted to assess its potential benefit in HF and left ventricular ejection fraction (LVEF)>40%, a population in whom treatment strategies effectively improving outcomes are scarce.

The goal of this trial is to assess the benefit of heart rate regularization through AV node ablation and conduction system pacing (CSP) in patients with permanent AF and HF with preserved or mildly reduced systolic function. The investigators hypothesize that heart rate regularization added to physiological pacing - preventing the deleterious effect of right apical pacing - reduces mortality, HF hospitalisations or worsening HF in these patients.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Permanent atrial fibrillation
  • At least one episode of hospitalisation due to heart failure in the previous 12 months.
  • Left ventricular ejection fraction > 40%
  • Average resting heart rate ≤ 110 beats per minute
  • NT-proBNP ≥ 900 pg/ml in the 30 days prior to enrollment
  • Age ≥ 18 years
  • Capacity to understand the nature of the study, legal ability and willingness to give informed consent.

Exclusion criteria

  • Severe frailty (Clinical Frailty Scale ≥ 7) or comorbidity reducing life expectancy to < 12 months.
  • Acute heart failure at the time of enrollment or systolic blood pressure < 80 mmHg in the absence of inotropic agents.
  • Severe chronic kidney disease (estimated Glomerular Filtration Rate ≤ 20 ml/1,73 m2
  • Severe mitral or aortic valvular heart disease
  • Anaemia (Haemoglobin < 10 g/dl)
  • Morbid obesity (BMI ≥ 35)
  • Severe Chronic Obstructive Pulmonary Disease (Gold ≥ 3)
  • Presence of a different indication for pacing of implantable cardioverter-defibrillator (ICD)
  • Obstructive hypertrophic cardiomyopathy
  • Infiltrative cardiomyopathy (amyloidosis, sarcoidosis, Fabry disease, others)
  • Simultaneous participation in a different trial

Treatment and study plan

Conduction System Pacing (pacemaker implantation)

Device

Conduction System Pacing (pacemaker implantation) and Atrioventricular node ablation

Other names: Atrioventricular node ablation

Primary outcomes

  1. Composite primary endpoint

    Time frame: 36 months

    All-cause mortality, heart failure hospitalisation and worsening heart failure

Secondary outcomes

  1. All-cause mortality

    Time frame: 36 months

    Mortality due to any cause

  2. Cardiovascular mortality

    Time frame: 36 months

    Mortality due to cardiovascular causes

  3. Heart failure hospitalization

    Time frame: 36 months

    Hospitalization due to heart failure decompensation

  4. Worsening heart failure

    Time frame: 36 months

    An episode of heart failure diagnosed based on symptoms, signs, imaging and analytical criteria that requires unplanned medical attention and intravenous diuretic therapy

  5. Unplanned cardiovascular hospitalisation

    Time frame: 36 months

    Unplanned cardiovascular hospitalisation

  6. Left ventricular ejection fraction

    Time frame: 12 months

    assessed by the Simpson method

  7. Change in left ventricular dimension

    Time frame: 12 months

    end-diastolic and end-systolic volumes

  8. Change in degree of mitral regurgitation

    Time frame: 12 months

    Change in degree of mitral regurgitation

  9. Change in functional status

    Time frame: 36 months

    Assessed by New York Heart Association (NYHA) on a I to IV scale (I being better functional status and IV worst possible functional status)

  10. Major adverse events during or in the first 30-days following pacemaker implantation

    Time frame: 30 days

    Percentage of patients suffering one of the following: death, cardiac tamponade, perforation requiring cardiac surgery, pneumothorax, haemothorax, device infection, endocarditis, lead displacement requiring re-intervention

  11. Major adverse events during or in the first 30-days following atrioventricular node ablation

    Time frame: 30 days

    Percentage of patients suffering one of the following: death, cardiac tamponade, perforation requiring cardiac surgery, puncture site vascular complications requiring vascular surgery

Study contacts

Contact information is provided by the study sponsor or research team.

Ana Isabel Castillo Varón, PhD

CONTACT

[email protected]

+34 917792742

Daniel Rodriguez Muñoz, MD, PhD

CONTACT

[email protected]

+34 917792742

Sponsors and collaborators

Lead sponsor

Daniel Rodríguez Muñoz

Other

Collaborators

  • Sociedad Castellana de Cardiologia

Registry information

Official study title

Conduction System PACing and Atrioventricular Node Ablation in Patients With hEart Failure, Left Ventricular Ejection Fraction >40% and Permanent Atrial FIBrilation: the PACE-FIB Trial

Acronym: PACE-FIB

Important dates

Study start
2022
Primary completion
2030
Study completion
2030
First posted
Aug 31, 2021
Registry last updated
Sep 9, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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