← Eichor
Study identifier: NCT05988411 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

ULTRA-HFIB-Redo: Ultrasound-based Renal Sympathetic Denervation vs Control in Redo Ablation Patients

Condition: Paroxysmal Atrial Fibrillation · Persistent Atrial Fibrillation  ·  Sponsor: Vivek Reddy

PhaseNA
Planned participants250
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a Prospective, controlled, single-blind, randomized (2:1, Intervention:Control) clinical trial. The purpose of the study is to determine the role of adjunctive renal sympathetic denervation in the prevention of Atrial Fibrillation (AF) recurrence in patients with hypertension scheduled for a redo AF ablation procedure for paroxysmal or persistent AF. Patients will be randomized to either i) AF ablation (Control) or ii) AF ablation + renal sympathetic denervation (Intervention).

This description comes directly from the study's public registry record.

Talk to the study team

Jeff Lam, MS  ·  (212) 824-8929  ·  jeff.lam@mountsinai.org

Betsy Ellsworth, MSN ANP  ·  (212) 824-8902  ·  betsy.ellsworth@mountsinai.org

Always discuss trial participation with your own doctor first.

Locations (8)

Arrhythmia Research GroupJonesboro, Arkansas, United StatesRecruiting
UCSFSan Francisco, California, United StatesRecruiting
Los Robles Medical CenterThousand Oaks, California, United StatesRecruiting
Henry Ford Health SystemDetroit, Michigan, United StatesRecruiting
Mount Sinai HospitalNew York, New York, United StatesRecruiting
Trident Medical CenterCharleston, South Carolina, United StatesRecruiting
ChristusTyler, Texas, United StatesRecruiting
Virginia Commonwealth UniversityRichmond, Virginia, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT05988411