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Paroxysmal Atrial FibrillationNCT04269785

Inflammatory and Endothelial Function Response, and Arrhythmia Recurrence Following Catheter Ablation for Atrial Fibrillation

A study testing Cryoballoon ablation and Radiofrequency ablation in people with Paroxysmal Atrial Fibrillation and Persistent Atrial Fibrillation, run by Karan Saraf.

Withdrawn

Withdrawn. The study stopped before anyone enrolled.

Official record
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Trial summary

Current international guidelines recommend a three-month blanking period after pulmonary vein isolation (PVI) for atrial fibrillation (AF). Early recurrence of atrial tachyarrhythmia (ERAT; comprising of AF, left atrial tachycardia and atrial flutter) is common, occurring in up to 65% of patients, but in the first… Read more about this study

Who is it for?
Ages 18 to 65 years
What is being tested?
Cryoballoon ablation and Radiofrequency ablation
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
0 participants
Where
No sites listed yet
Study dates
30 Jan 2023to 1 Jun 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age 18-75 years
  • Paroxysmal AF or persistent AF of less than 6 months' duration
  • Structurally normal heart on transthoracic echocardiogram other than mild left atrial dilatation (<34ml/m2, indexed to body surface area)
  • Due to undergo pulmonary vein isolation on clinical grounds

Who cannot join

  • Known genetic/inherited disorder that predisposes to atrial fibrillation, or Brugada syndrome
  • Metabolic syndrome as defined by National Cholesterol Education Program (NCEP) Adult Treatment Panel III (ATP III) criteria
  • Obesity (BMI>40)
  • Inability or unwillingness to receive oral anticoagulation with a vitamin K antagonist (VKA) or non-VKA oral anticoagulant (NOAC)
  • Known atrial flutter
  • Ischaemic heart disease documented by coronary or CT angiography, or confirmed history of myocardial infarction
Show all 19Show fewer
  • Current stage II or III hypertension (diastolic BP >100mmHg, systolic BP>160mmHg) confirmed on serial readings or ambulatory monitoring
  • Diabetes mellitus other than diet controlled
  • Previous catheter or surgical ablation procedure for AF
  • Unwillingness or inability to complete the required follow-up arrangements
  • Persistent AF > 6 months' duration or permanent AF
  • Prior prosthetic heart valve replacement or structural cardiac abnormality including moderate or severe heart valve disease
  • Moderate or severe left atrial dilatation
  • Known infiltrative cardiomyopathy
  • Known left ventricular systolic dysfunction (ejection fraction <45%)
  • Pregnancy
  • Co-morbidities known to be associated with an inflammatory response (eg. Rheumatoid arthritis)
  • Unexplained baseline elevation of ESR or CRP above the normal lab reference ranges
  • Additional ablation lesions beyond pulmonary vein isolation

About this study

Official title: Post-ablation Inflammatory Response and Endothelial Function in the Development of Early Recurrence of Atrial Tachyarrhythmia After Pulmonary Vein Isolation; Implications for Pulmonary Vein Reconnection and Freedom From Atrial Fibrillation

Current international guidelines recommend a three-month blanking period after pulmonary vein isolation (PVI) for atrial fibrillation (AF). Early recurrence of atrial tachyarrhythmia (ERAT; comprising of AF, left atrial tachycardia and atrial flutter) is common, occurring in up to 65% of patients, but in the first month is generally thought not to predict long-term AF recurrence, and re-intervention is not recommended. Suggested causes for ERAT include inflammation and arrhythmogenic structural changes caused by ablation lesions. Early, purely inflammatory ERAT would not lead to late AF recurrence as pulmonary vein reconnection is established as the main factor associated with long-term recurrence in paroxysmal AF. Previous studies have shown ERAT in the second to third month (rather than first month) to be a stronger predictor of late AF recurrence, due to presumed reduction in the contribution of the acute inflammatory response after this. Biochemical data have shown that the post-ablation inflammatory phase is usually limited to the first month after both radiofrequency (RF) and cryoballoon (CB) ablation, though inflammatory markers have been shown to be less elevated following CB PVI. Histologically, lesions formed by the two modalities differ significantly. RF lesions are characterised by irregular boundaries and significant disruption to the endothelium, exposing the sub-endothelial layer and resulting in significant and sustained platelet activation, changes which can last for many months. CB lesions on the other hand, are observed as well demarcated and homogenous within one week, with reduced thrombogenicity, which may lead to reduced inflammation. ERAT following CB ablation cannot be accurately predicted by inflammatory response and it is postulated that endothelial function may play a role in the development of ERAT in such patients. Some studies have shown reduced recurrence rate and re-hospitalisation amongst the CB population, including the FIRE and ICE trial, potentially resulting in a better patient experience with CB and the possibility of a shorter blanking period. Post-ablation inflammatory response is more predictive of ERAT following RF than CB PVI, and the latter is considered to be associated with less inflammation. There is however, a paucity of data evaluating endothelial function post-AF ablation and its correlation with ERAT or late recurrences of arrhythmia. Given that earlier re-intervention in patients with ERAT in the third month of the blanking period can result in greater outcomes with respect to late recurrence of AF, if it can be demonstrated that endothelial function testing in the first few months post-CB PVI can be predictive of later ERAT, then shortening the blanking period following CB PVI and performing repeat ablation to control troublesome later ERAT may reduce overall patient morbidity and re-hospitalisation.

The purpose of this novel pilot study is to examine the relationship between the post-ablation inflammatory response, endothelial function and timing and frequency of ERAT for patients undergoing RF and CB PVI for paroxysmal or short-lived persistent (less than 6 months' duration) AF. If the initial data provides hypothesis generating information, the aim would be to perform the study on a larger basis with higher statistical power to determine whether early post-ablation endothelial function testing can predict recurrences and identify those suitable for earlier re-intervention.

Being tested
Cryoballoon ablation, Radiofrequency ablation
Keywords
atrial fibrillation, ablation, radiofrequency, cryoballoon, inflammation, endothelial function, recurrence
Medical subject headings
Atrial Fibrillation, Inflammation, Recurrence

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Cryoballoon ablationDevice

    Ablation aimed at performing pulmonary vein isolation for atrial fibrillation using cryoballoon catheter (cold therapy)

  • Radiofrequency ablationDevice

    Ablation aimed at performing pulmonary vein isolation for atrial fibrillation using radiofrequency catheter (heat therapy)

Study groups in NCT04269785
Study groupRoleWhat they receive
Radiofrequency ablationActive comparatorThese patients will receive ablation by radiofrequency catheter, guided by of 3-dimensional electro-anatomic mapping technology
Receives: Device: Radiofrequency ablation
Cryoballoon ablationActive comparatorThese patients will receive ablation by cryoballoon catheter, guided by X-ray fluoroscopy
Receives: Device: Cryoballoon ablation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Incidence of recurrence of atrial arrhythmia in the 3 months following ablation

    Whether patients have experienced a recurrence of atrial arrhythmia (AF, left atrial flutter or left atrial tachycardia) in the 3 months following their ablation

    Measured: 3 months

Secondary outcomes (2)
  1. Rate and degree of rise of inflammatory markers in the 3 months following ablation

    Inflammatory blood markers such as CRP

    Measured: 3 months

  2. Degree of endothelial dysfunction in the 3 months following ablation (EndoPAT testing)

    Endothelial function measured using the EndoPAT technology

    Measured: 3 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted17 Feb 2020
  2. Study start30 Jan 2023 (estimated)
  3. Primary completion30 Jan 2024 (estimated)
  4. Study completion1 Jun 2024 (estimated)

Why it stopped: Funding

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
20 patients with paroxysmal AF or short-lived persistent AF (less than 6 months' duration), randomised to receive ablation by radiofrequency (RF) or cryoballoon (CB) in a 1:1 allocation.
Masking
None (open label)
Enrolment
0 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04269785
Sponsor's protocol ID
262517
Status last verified
Oct 2023
First submitted
23 Jan 2020
Last updated
1 Nov 2023
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Cryoballoon ablation and Radiofrequency ablation in people with Paroxysmal Atrial Fibrillation and Persistent Atrial Fibrillation, run by Karan Saraf.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 19 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: withdrawn, as of the sponsor's last update on 1 Nov 2023. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was withdrawn before enrolling participants, so there are no results.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Incidence of recurrence of atrial arrhythmia in the 3 months following ablation (time frame: 3 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Nov 2023.

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