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

Recruiting now · Not applicable

Conditions studied: Intra-Abdominal Hypertension

In brief

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.

Key facts

Study ID

NCT06876896

Run by

Wake Forest University Health Sciences

People needed

50

Starts

2026-03-03

Expected to finish

2026-12-30

Last updated by the study team

2026-03-19

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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.

You may not qualify if…

• 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

Where it is running

• Wake Forest Health Sciences — Winston-Salem, North Carolina, United States (enrolling)

Full record on ClinicalTrials.gov

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