Clinical Trial

Prevention of Edema After Coronary Artery Bypass Graft by Customized Pressure-guided Elastic Bandages

Study acronym: PEACCE
Recruiting
View on ClinicalTrials.gov →
Record status
This record was last updated February 9, 2026 (before its estimated March 31, 2026 completion). Its status may not reflect the trial's current state.
Summary
The study aimed to assess the efficacy of customized pressure-guided elastic bandages (CPG-EB) in preventing postoperative edema and complications in Coronary Artery Bypass Graft (CABG) patients. While compression therapy, like compressive stockings, has benefits in preventing edema, concerns about affordability persist. CPG-EB provides optimal sub-bandage pressure, proven effective in venous leg ulcers. Implementing CPG-EB post-CABG could enhance venous blood flow, reducing complications and improving outcomes. Patients were divided into two groups: one with CPG-EB and the other standard post-CABG care. Data collected at 1, 2, and 6 weeks post-surgery assessed swelling and wound complications. Comparative analysis used standardized criteria.
Protocol Amendment History 5 amendments
This ClinicalTrials.gov record has been amended 5 times since 2024-09-16; most recent amendment 2026-02-06.
Status change: Not Yet Recruiting → Recruiting 2025-02-10
Trial Details
NCT Number NCT06603961
Lead Sponsor Siriraj Hospital
Conditions Limb Edema, Surgical Site Infections, Leg Swelling, Compression Bandages, Coronary Artery Bypass Graft, CABG, Saphenectomy, Saphenous Vein +3 more
Enrollment 106 participants
Start Date 2025-01-19
Primary Completion 2026-03-31 (estimated)
Study Completion 2026-05-31 (estimated)
Updated on ClinicalTrials.gov 2026-02-09