← Eichor
Study identifier: NCT05029570 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Heart Rate Regularization in Atrial Fibrilation and Heart Failure

Condition: Heart Failure · Atrial Fibrillation  ·  Sponsor: Daniel Rodríguez Muñoz

PhaseNA
Planned participants334
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Daniel Rodriguez Muñoz, MD, PhD  ·  +34 917792742  ·  danielantonio.rodriguez@salud.madrid.org

Ana Isabel Castillo Varón, PhD  ·  +34 917792742  ·  aicastillo.imas12@h12o.es

Always discuss trial participation with your own doctor first.

Locations (1)

Hospital Universitario 12 de OctubreMadrid, Madrid, SpainRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT05029570