Cavo-Tricuspid Isthmus Block Durability After Pulsed Electric Field Ablation
Recruiting
N/AInterventional Study
Flutter, AtrialCavotricuspid Isthmus Dependent Right Atrial FlutterCatheter Ablation
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
150 (estimated)
Sponsor
Institute for Clinical and Experimental Medicine · Government
Who this trial is looking for
This trial is looking for adults with atrial flutter who are having catheter ablation. Participants will help researchers understand the effectiveness of a specific treatment and how long to wait after treatment before checking heart function.
Are You a Good Fit for This Trial?
You may be able to join if
I am at least 18 years old.
I have been diagnosed with atrial flutter.
I am undergoing catheter ablation for my condition.
I am willing to sign informed consent.
You may not be able to join if
I have a left atrium diameter greater than 65 mm.
I have had a CTI ablation in the past.
I have had heart valve surgery.
I have significant heart valve problems.
I am pregnant or breastfeeding.
I have a life expectancy of less than one year.
I have uncorrected congenital heart disease.
I have active myocarditis.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
This study seeks to assess the acute durability of the CTI block when PEF energy is used. Second goal is to establish the optimal waiting time for the conduction recovery after PEF CTI ablation and to assess the utility of routine adenosine testing for dormant conduction. Moreover, this study aims to investigate the differences in acute efficacy and adverse events (hemolysis, coronary vasospasm) b…
This study seeks to assess the acute durability of the CTI block when PEF energy is used. Second goal is to establish the optimal waiting time for the conduction recovery after PEF CTI ablation and to assess the utility of routine adenosine testing for dormant conduction. Moreover, this study aims to investigate the differences in acute efficacy and adverse events (hemolysis, coronary vasospasm) between the two available configurations (basket or flower) of the pentaspline Farawave catheter (Farapulse-Boston Scientific Inc, USA).
Trial Locations
Loading…
Loading trial locations…
Facility
City
State
Country
Status
Eligibility Criteria
Inclusion Criteria:
* patients with paroxysmal AF undergoing PVI by PEF energy with documented typical atrial flutter or patients with persistent AF in whom catheter ablation of CTI is planned as a part of a complex procedure
* Age ≥ 18 years at the time of study enrollment
* Signed informed consen…
Inclusion Criteria:
* patients with paroxysmal AF undergoing PVI by PEF energy with documented typical atrial flutter or patients with persistent AF in whom catheter ablation of CTI is planned as a part of a complex procedure
* Age ≥ 18 years at the time of study enrollment
* Signed informed consent
Exclusion Criteria:
* \- LA diameter \> 65 mm (measured in the parasternal long-axis view)
* History of CTI ablation in the past
* History of cardiac valve surgery
* Significant valvular defect
* Age below 18 years
* Pregnancy, breastfeeding
* Any disease with a life expectancy \<1 year
* Uncorrected congenital heart disease or valvular obstruction
* Active myocarditis
* Untreated hypothyroidism or hyperthyroidism
* Recipient of any major organ transplant (e.g., lung, liver, heart)
* HIV positivity with a survival expectancy of less than five years due to HIV
* Chronic dialysis treatment
* Unwillingness to participate.
Contacts
No contact information available.
What are you hoping to find?
Picking one helps us show the most relevant trials first.
Your results are loading in the background — you can
change this any time from the results page.
Set your location to continue
Find My Trials uses your location to surface clinical trials near you.
Add your city or zip code to your profile and try again.