Impact of Prontosan Wound Gel X on Surgical Site Infections in Cardiac Surgery
Recruiting
Observational Study
Surgical Site Infection After Major Surgery
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 456 (estimated)
- Sponsor
- IRCCS Policlinico S. Donato · Other
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About This Trial
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 …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Scheduled for elective cardiac surgery requiring median sternotomy (e.g., CABG, valve surgery, aortic surgery)
* Ability to provide informed consent
* Independent clinical decision by the treating surgeon to apply Prontosan Wound Gel X during surgery, irrespective of study enr…
Contacts