Actively Recruiting

Phase Not Applicable
Age: 18Years - 85Years
All Genders
NCT04664686

Rate or Rhythm Control in CRT: the RHYTHMIC Study

Led by Guy's and St Thomas' NHS Foundation Trust · Updated on 2026-01-26

70

Participants Needed

1

Research Sites

310 weeks

Total Duration

On this page

Sponsors

G

Guy's and St Thomas' NHS Foundation Trust

Lead Sponsor

K

King's College London

Collaborating Sponsor

AI-Summary

What this Trial Is About

70 patients with heart failure, AF and CRT with BiV\<95% will be randomised to either AF ablation or AV node ablation. Evaluation at 6 months with echocardiography and clinical assessment.

CONDITIONS

Official Title

Rate or Rhythm Control in CRT: the RHYTHMIC Study

Who Can Participate

Age: 18Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Ability to provide informed consent and willing to follow the study plan and follow-up
  • QRS duration greater than 120ms on ECG, left ventricular ejection fraction of 35% or less, and heart failure symptoms (NYHA class II-IV) at time of CRT implant or upgrade
  • Successful CRT implant or upgrade including an atrial lead
  • Biventricular pacing less than 95% due to atrial fibrillation at least 3 months after CRT implant or upgrade
  • Clinically indicated for AV node ablation
Not Eligible

You will not qualify if you...

  • Life expectancy less than 1 year
  • Presence of atrial or ventricular blood clot
  • Permanent atrial fibrillation
  • Mechanical aortic valve replacement
  • Severe peripheral vascular disease
  • Female participants who are pregnant, breastfeeding, or planning pregnancy during the study
  • Participation in other studies involving active treatment or investigational therapies

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Guys and St Thomas' NHS Foundation Trust

London, United Kingdom, SE1 7EH

Actively Recruiting

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Research Team

C

Christopher A Rinaldi

CONTACT

F

Felicity de Vere

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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