Triclosan-antibacterial Sutures Efficacy on the Incidence of Surgical Site Infection in Clean-contaminated Wounds
Launched by CLINAMYGATE · Feb 4, 2020
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying the effectiveness of sutures coated with an antibacterial agent called Triclosan in reducing the risk of surgical site infections (SSI) in patients undergoing clean-contaminated wound surgeries. Clean-contaminated wounds are those that may be at some risk of infection, such as surgeries involving the digestive or respiratory tracts. The trial aims to compare the rate of infections in patients who receive stitches coated with Triclosan versus those who receive standard stitches without this coating.
To participate in the trial, individuals should be between the ages of 18 and 75 and scheduled for clean-contaminated wound surgery. However, certain patients are not eligible, including those with weakened immune systems or those undergoing treatments that suppress the immune system, as well as patients who already have an infection before surgery. If you join the trial, you will receive either the Triclosan-coated sutures or the standard sutures, and researchers will monitor you to see if the type of suture affects your chances of developing an infection. This study is currently recruiting participants, and your involvement could help improve surgical care for future patients.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • age: 18-75
- • clean-contaminated wound surgery
- Exclusion Criteria:
- • Patient has immunodeficiency disorder.
- • Patient receiving anti-cancer / immunosuppressive therapy.
- • Patients with established pre-operative infection whether community acquired or hospital acquired either at / remote from the operative site.
About Clinamygate
Clinamygate is a leading clinical trial sponsor dedicated to advancing medical research and innovation through the development and management of comprehensive clinical studies. With a focus on enhancing patient outcomes and accelerating the drug development process, Clinamygate collaborates with a diverse range of stakeholders, including pharmaceutical companies, research institutions, and healthcare providers. Our commitment to ethical practices and regulatory compliance ensures the highest standards of safety and efficacy in all trials. By leveraging cutting-edge technologies and a robust network of clinical sites, Clinamygate aims to bring transformative therapies to market efficiently and effectively, ultimately improving global health.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Giza, , Egypt
Patients applied
Trial Officials
Emad R Issak, Diploma
Study Director
ClinAmygate
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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