Compartment Syndrome Clinical Trials

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Comparative Study of Intra-abdominal Pressure Using Accuryn Monitoring System During Pulsed Field Ablation (PFA) for Treatment of Atrial Fibrillation and/or Atrial Flutter Under Sedation.

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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.

Locations
United States
North Carolina
Wake Forest Health Sciences
RECRUITING
Winston-salem
Contact Information
Primary
Karuna Rajkumar, MD
kputturr@wakehealth.edu
832-707-0858
Time Frame
Start Date: 2026-03-03
Estimated Completion Date: 2026-12-30
Participants
Target number of participants: 50
Treatments
Experimental: Accuryn Foley catheter placement
foley catheter is made to measure intra-abdominal pressure
Sponsors
Leads: Wake Forest University Health Sciences

This content was sourced from clinicaltrials.gov