Prophylactic Effects for Preventing Surgical Site Infection in Third Molar Surgery
Launched by UJI TAKEDA HOSPITAL · Apr 12, 2024
Trial Information
Current as of November 14, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is looking into how effective a specific antibiotic, ampicillin, is in preventing infections after surgery to remove wisdom teeth, known as third molars. The researchers want to find out if giving this antibiotic for different lengths of time can help reduce the chances of getting an infection at the surgery site.
To be part of this study, participants need to be at least 20 years old and scheduled to have their wisdom teeth removed in a hospital setting under sedation. They should also be in generally good health, as determined by the American Society of Anesthesiologists. However, people who are pregnant, allergic to ampicillin, or have certain health issues that increase their risk for infection will not be eligible. If you join the study, you can expect to follow a specific treatment plan and contribute to important research that could help improve surgical care for others in the future.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Minimum age of 20 years
- • American Society of Anesthesiologists (ASA) physical status of 1
- • Planned extraction of bilateral mandibular third molar with the necessity of bone removal based on panoramic radiography in an inpatient setting under IV sedation
- • Agreement to follow the study protocol
- Exclusion Criteria:
- • Pregnancy or suspicion of pregnancy
- • Allergy and/or contraindication to ampicillin
- • History of a known SSI risk factors, such as diabetes, steroid or immunosuppressant use, and endocarditis
- • Receiving any antibiotic therapy
- • Active infection of the third molars with pus, edema, and trismus
About Uji Takeda Hospital
Uji Takeda Hospital is a leading healthcare institution dedicated to advancing medical research and patient care through innovative clinical trials. Located in Uji, Japan, the hospital specializes in a range of therapeutic areas, focusing on developing cutting-edge treatment options to improve patient outcomes. With a commitment to high ethical standards and rigorous scientific methodology, Uji Takeda Hospital collaborates with esteemed researchers and pharmaceutical partners to facilitate groundbreaking studies that contribute to the global medical community. The hospital's state-of-the-art facilities and multidisciplinary approach ensure a comprehensive and patient-centered experience throughout the clinical trial process.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Uji, Japan
Patients applied
Trial Officials
Keita Kano, PhD
Study Chair
Uji Takeda Hospital
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported