Decolonization Efficacy of Polyhexanide vs. Mupirocin
Launched by SWISS PARAPLEGIC RESEARCH, NOTTWIL · Oct 8, 2024
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is looking at a new approach to help reduce the presence of a bacteria called Staphylococcus aureus, which can sometimes cause infections. The study compares two different treatments: one using a product called polyhexanide and the other using a standard treatment of mupirocin (an antibiotic) combined with chlorhexidine (a disinfectant). The goal is to see if the polyhexanide treatment can be as effective or better in helping patients who are scheduled for elective spine surgery and are already carrying this bacteria. The trial will involve 24 participants who will be divided into two groups to receive one of the treatments.
To be part of this trial, participants must be over 18 years old, scheduled for elective spine surgery, and have Staphylococcus aureus on their skin or in their nose. However, those who are having emergency surgery, are allergic to the treatments, or have certain other health issues won’t be eligible. During the trial, participants can expect to receive one of the treatments and will be monitored for how well it works and how they tolerate it. Importantly, this study is not yet recruiting participants, but it aims to help find better ways to prevent infections in surgical patients.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Age over 18 years
- • Scheduled for elective spinal surgery
- • Colonized with Staphylococcus aureus
- • Informed consent provided
- Exclusion Criteria:
- • Emergency spine surgery
- • Methicillin-resistant Staphylococcus aureus (MRSA) or mupirocin-resistant S. aureus
- • Known allergies to products used in the trial
- • Pregnant or breastfeeding women
- • Recent antibiotic therapy (within 14 days)
- • Known non-compliance, substance abuse, or psychological disorders
- • Participation in another antimicrobial trial within the last 30 days
About Swiss Paraplegic Research, Nottwil
Swiss Paraplegic Research (SPER) in Nottwil is a leading institution dedicated to advancing the understanding and treatment of spinal cord injuries and related conditions. As a prominent clinical trial sponsor, SPER focuses on innovative research that aims to improve the quality of life for individuals affected by paralysis. The organization collaborates with a network of academic and clinical partners to conduct rigorous studies, translating scientific discoveries into practical therapies and rehabilitation strategies. With a commitment to excellence and patient-centered care, SPER plays a vital role in shaping the future of spinal cord injury research and rehabilitation.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Nottwil, Lucerne, Switzerland
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported