Condition: Surgical Site Infection After Major Surgery · Sponsor: IRCCS Policlinico S. Donato
This study aims to evaluate the effects of Prontosan® Wound Gel X on the incidence of superficial surgical site infections (SSI) in adult patients undergoing elective cardiac surgery with median sternotomy. The primary objective is to assess how the intraoperative application of the gel impacts the occurrence of SSIs, defined according to CDC/NHSN criteria. Secondary objectives include evaluating the length of hospital stay, the incidence of unplanned re-operations, and identifying any latent clinical subgroups through clustering analysis. The study will be conducted as a prospective, single-center, observational, post-market trial. The primary endpoint will be the incidence of SSIs during the post-operative hospitalization period, while secondary endpoints will focus on hospital stay duration, re-operation rates, and feasibility indicators such as adherence to the protocol and completeness of data collection. The study also includes an exploratory endpoint where hierarchical clustering will be used to identify clinical subgroups based on demographic, clinical, and procedural variables. Up to 456 adult patients will be enrolled, all of whom are undergoing elective cardiac surgery via median sternotomy at IRCCS Policlinico San Donato. The inclusion criteria include patients aged 18 or older, scheduled for surgery, and able to provide informed consent, with the clinical decision to use Prontosan® Wound Gel X during the surgery. Exclusion criteria involve urgent surgeries, par…
This description comes directly from the study's public registry record.
Gianluca Castiello, MSc, RN · +39 02 5277 4236 · gianluca.castiello@grupposandonato.it
Giacomo Bortolussi, MD · +39 02 5277 4236 · giacomo.bortolussi@grupposandonato.it
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| IRCCS Policlinico San Donato | San Donato Milanese, Michigan, Italy | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07275307