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Renal Denervation + AF Ablation for Atrial Fibrillation (ULTRA-HFIB Trial)
N/A
Waitlist Available
Led By Vivek Reddy, MD
Research Sponsored by Vivek Reddy
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Age ≥ 18
Planned for a first-ever AF ablation procedure (paroxysmal or persistent) with technically successful AF ablation procedure completed prior to randomization
Must not have
Individual with valvular AF or AF due to a reversible cause
Individual has a single functioning kidney (either congenitally or iatrogenically)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 months
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing whether adding a renal sympathetic denervation procedure to standard AF ablation can help prevent AF recurrence.
Who is the study for?
This trial is for adults over 18 with a history of high blood pressure and planned first-ever AF ablation procedure. They must be willing to follow the study plan and have controlled hypertension, either Stage III or on medication. Excluded are those with long-term persistent AF, severe heart failure, poor kidney function, known allergies to contrast media not treatable, pregnant or nursing women, single functioning kidney individuals, drug/alcohol dependency issues, concurrent enrollment in conflicting trials.
What is being tested?
The ULTRA-HFIB Pilot aims to see if adding renal denervation (RDN) to standard atrial fibrillation (AF) ablation helps prevent AF from coming back. Participants will be randomly assigned to just get an AF ablation or both an AF ablation and RDN.
What are the potential side effects?
Potential side effects may include reactions related to catheter insertion such as bleeding or bruising at the site of entry, damage to blood vessels near the kidneys during RDN treatment; however specific side effects will depend on individual patient responses.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am 18 years old or older.
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I am scheduled for my first AF ablation procedure and it must be completed successfully before I can join.
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I have high blood pressure and am on medication for it.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
My AFib is caused by a heart valve issue or a temporary condition.
Select...
I have only one working kidney.
Select...
I have had atrial fibrillation for more than a year.
Select...
I have had a procedure to correct heart rhythm problems before.
Select...
I cannot have AF catheter ablation due to a heart clot or issues with blood thinners.
Select...
I am not pregnant or nursing.
Select...
My kidney function is reduced, with an eGFR below 40.
Select...
I have severe heart failure.
Select...
I have high blood pressure caused by another health condition.
Select...
I have a chronic condition like Crohn's disease or ulcerative colitis.
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My kidney's blood vessels are not suitable for the treatment based on an angiography.
Select...
I have had surgery on the left side of my heart.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Single-procedure freedom from AT/AF/AFL recurrence ≥ 30 seconds
Secondary study objectives
AF burden at 12 months
AF burden at 6 months
Change in office systolic blood pressure change from baseline to 12 months
+3 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Catheter ablation + renal denervationExperimental Treatment2 Interventions
Catheter ablation + renal denervation
Group II: Catheter ablation onlyActive Control1 Intervention
Catheter ablation
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
renal denervation
2011
N/A
~60
Catheter ablation
2016
Completed Phase 4
~1220
Find a Location
Who is running the clinical trial?
Vivek ReddyLead Sponsor
20 Previous Clinical Trials
5,187 Total Patients Enrolled
10 Trials studying Atrial Fibrillation
906 Patients Enrolled for Atrial Fibrillation
Vivek Reddy, MD3.816 ReviewsPrincipal Investigator - Icahn School of Medicine at Mount Sinai
Icahn School of Medicine at Mount Sinai
34 Previous Clinical Trials
12,984 Total Patients Enrolled
19 Trials studying Atrial Fibrillation
7,550 Patients Enrolled for Atrial Fibrillation
5Patient Review
I had a great experience with Dr. Reddy. Not only did he attend to all of my medical concerns, but he also was able to fix my A Fib. I'm very grateful.
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I do not have a current drug or alcohol problem and can follow study instructions.I am 18 years old or older.I have a history of high blood pressure.I am scheduled for my first AF ablation procedure and it must be completed successfully before I can join.My AFib is caused by a heart valve issue or a temporary condition.I have only one working kidney.You are expected to live less than one year due to a medical condition.I have had atrial fibrillation for more than a year.I have high blood pressure and am on medication for it.I have had a procedure to correct heart rhythm problems before.I cannot have AF catheter ablation due to a heart clot or issues with blood thinners.I am not pregnant or nursing.My kidney function is reduced, with an eGFR below 40.I have severe heart failure.You are allergic to contrast dye and cannot be treated for the allergy.I have high blood pressure caused by another health condition.I have a chronic condition like Crohn's disease or ulcerative colitis.You have used other devices to treat high blood pressure before, such as the ROX Coupler, Mobius stent, or the CVRx barostimulator device.My kidney's blood vessels are not suitable for the treatment based on an angiography.I have had surgery on the left side of my heart.I've had a heart attack, unstable chest pain, stroke, or heart failure hospital visit in the last 3 months.
Research Study Groups:
This trial has the following groups:- Group 1: Catheter ablation only
- Group 2: Catheter ablation + renal denervation
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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