RecruitingNot Applicable

Intra-abdominal Pressure (IAP) During PFA Treatment of A-fib/ A-Flutter

United States50 participantsStarted 2026-03-03

Plain-language summary

The purpose of this study is to investigate the intra-abdominal pressure utilizing the Accuryn monitoring system during pulsed field ablation procedures in the electrophysiology lab compared to the type of anesthetic utilized.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Adult patients receiving pulse field ablation procedures for standard of care treatment of atrial fibrillation and/or atrial flutter. * Eligible for Foley catheter placement with no contraindications to Intra-abdominal pressure (IAP) monitoring. Exclusion Criteria: * Patients under the age of 18 will be excluded. * History of intra-abdominal surgery within the past 6 months. * Known contraindications to bladder catheterization or catheter ablation; history of prostate issues / Benign prostatic hyperplasia (BPH) or frequent urinary tract infections * Pregnant or breastfeeding individuals * History of chronic obstructive pulmonary disease (COPD) with home oxygen use

What they're measuring

Intra-abdominal pressure under Pulsed Field Ablation (PFA) under general anesthesia

Timeframe: hour 2

Intra-abdominal pressure under Pulsed Field Ablation (PFA) under sedation

Timeframe: hour 2

Trial details

NCT IDNCT06876896

SponsorWake Forest University Health Sciences

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-12-30

Contact for this trial

Karuna Rajkumar, MD

832-707-0858 kputturr@wakehealth.edu

View on ClinicalTrials.gov More Intra-Abdominal Hypertension trials