Clinical Trial

Use of Platelet-Rich Plasma to Reduce Sternal Wound Complications After CABG With Median Sternotomy

Completed
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Summary
The goal of this clinical trial is to learn whether applying autologous platelet-rich plasma (PRP) to the sternal wound during heart surgery improves wound healing and reduces complications after surgery. The study also aims to evaluate whether PRP can reduce hospital-related outcomes and costs. The main questions this study aims to answer are: Does the use of PRP reduce superficial \& deep sternal wound infections and rate of readmissions? Does PRP improve wound healing after heart surgery? Does PRP reduce the cost of hospitalization and length of ICU stay. Does PRP reduce the requirement of red cell concentrate (RCC) and platelets to less than 4 units each Researchers will compare PRP applied to the sternal wound before closure with standard sternal wound closure alone to determine whether PRP provides additional benefit beyond standard surgical care. Participants were randomly assigned to one of two groups. Participants will: Receive standard sternal wound closure or PRP applied to the sternal wound followed by standard closure Be monitored for wound infections and healing outcomes after surgery Have hospital cost, RCC \& platelet units used, ICU stay, and readmission data recorded during the postoperative period Patients and outcome assessors were blinded to the treatment assignment. Surgeons were aware of the intervention due to the nature of the procedure. This study aims to determine whether adding PRP to standard sternal closure can improve recovery and reduce complications following cardiac surgery.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-01-11.
Trial Details
NCT Number NCT07352020
Lead Sponsor Shaheed Zulfiqar Ali Bhutto Medical University
Conditions Surgical Site Infection (SSI), Mediastinitis, Delayed Wound Healing
Enrollment 98 participants
Start Date 2022-07-07
Primary Completion 2023-01-07 (estimated)
Study Completion 2023-02-28 (estimated)
Updated on ClinicalTrials.gov 2026-01-27