Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07047235

Substrate Remodelling and Targeted Ablation in AF

Atrial fibrillation (AF) is the most common heart rhythm disorder, affecting millions worldwide and causing symptoms such as palpitations, fatigue and breathlessness. It also increases the risk of stroke and heart failure, so effective treatment is essential.

A treatment for AF involves catheter ablation, a minimally invasive procedure where problematic areas of the heart are targeted using controlled energy. This is done by passing wires called catheters, through blood vessels at the top of the leg all the way to the heart. However, this isn't effective for everyone and approximately half of patients experience a return of AF despite treatment.

In this researcher-led study at St Bartholomew's Hospital , the investigators will use a method called electroanatomical mapping to make a 3D picture of the left atrium, the heart's upper left chamber. To make this picture more detailed, information will be collected - such as how strong electrical signals are (voltage), how fast and in which direction they travel through the heart to describe abnormal areas and areas of scar within the heart. Information will also be gathered about the routes electricity takes and the nerve activity in the heart muscle. These detailed maps will help to understand why AF can continue indefinitely in some people, why ablation works for some people and not others, and improve how ablations are done to make them more effective.

All participants will undergo catheter ablation with these mapping methods integrated into the procedure. If AF recurs, patients will be invited for a second ablation targeting specific abnormal areas depending on the amount of scar found. This will be standardised across patients.

Patients will be followed for 12 months, with structured visits at 3, 6, 9 and 12 months and 48-hour ECG recorders at 6 and 12 months. By tracking how the heart's structure and electrical behaviour evolve, the aim is to to see if map-guided ablation reduces the need for further procedures, lowers healthcare costs and improves quality of life.

Ultimately, this study will provide clear, reproducible insights into AF mechanisms and yield practical guidance so clinicians can predict who will benefit from standard ablation treatment and who may require extra, map-guided treatment.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

St Bartholomew's Hospital

London, United Kingdom

Location status: Recruiting

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Able and willing to provide written informed consent
  • Age: 18 years or older
  • Clinical diagnosis: Persistent atrial fibrillation
  • Treatment status: Scheduled to undergo first-time catheter ablation for persistent AF

Exclusion criteria

  • Inability or unwillingness to provide informed consent
  • Under 18 years of age
  • Previous left atrial ablation for AF or other atrial arrhythmias
  • Any clinical contraindications to undergoing AF catheter ablation

Treatment and study plan

Pulmonary vein reisolation

Procedure

The pulmonary veins will be checked electrically and further ablation will be undertaken if they are not isolated.

Ganglionic plexi ablation

Procedure

Sites where ganglionix plexi have been found will be ablated.

Substrate ablation

Procedure

Areas of rate dependent conduction velocity slowing will be targeted using cathether ablation

Primary outcomes

  1. Assessment of Electrical, Structural and Autonomic Remodelling in Persistent Atrial Fibrillation

    Time frame: 4 years

    A primary objective of this study is to delineate the remodelling changes that occur in persistent atrial fibrillation and to utilise these to develop tailored ablation strategies.

  2. Establish a Predictive Model to Idenitfy Which Patients are Responders to Pulmonary Vein Isolation Alone and Who Will Require Further Tailored Ablation Strategies

    Time frame: 24 months

    Based on clinical data approximately only 50% of patients with persistent atrial fibrillation who undergo pulmonary vein isolation remain in sinus rhythm. A main aim of the study is to develop a method to identify which patients will respond to pulmonary vein isolation alone and who will require further tailored ablation strategies.

  3. To Assess if Ablation of Rate Dependent Conduction Velocity Slowing Sites Improves Freedom from Atrial Fibrillation

    Time frame: 5 years

    All patients who recur after their initial ablation will be invited to undergo a repeat ablation procedure. All patients will undergo ganglionic plexi ablation and reisolation their pulmonary veins. Those who have low voltage zones of more than 30% of their total left atrium will undergo further ablation of rate dependent conduction velocity slowing sites.

Secondary outcomes

  1. Develop Personalised Electrical Atrial Models

    Time frame: 5 years

    The data taken from the electrophysiological procedures will be used to create mathematical computer models that can be used as an environment to test electrophysiological theories and response to ablation.

Study contacts

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

Sayed Al-Aidarous, MBBS, MRCP

CONTACT

[email protected]

Shohreh Honarbakhsh, MBBS, MRCP, PhD

CONTACT

[email protected]

02037658682

Sponsors and collaborators

Lead sponsor

Barts & The London NHS Trust

Other

Registry information

Official study title

Understanding Substrate Evolution in Persistent Atrial Fibrillation to Develop Tailored Ablation Strategies

Acronym: STRATA-AF

Important dates

Study start
2025
Primary completion
2029
Study completion
2030
First posted
Jul 2, 2025
Registry last updated
Nov 18, 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.

Published trials that share one or more normalized conditions with this study.