Valacyclovir in Pain Management of Acute Apical Abscesses
Launched by UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · Mar 2, 2022
Trial Information
Current as of July 12, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying the use of a medication called valacyclovir to help manage pain in patients with a condition known as acute apical abscesses, which are painful infections at the tip of a tooth root. The trial aims to evaluate the effectiveness of this medication in reducing pain before and after dental procedures, as well as to see how well the infection heals over time. Researchers plan to include 250 patients who are at least 18 years old and in good overall health, with clear evidence of tooth infection and moderate or severe pain.
Participants in the study will undergo dental treatments, including cleaning the infected area and possibly draining any abscess, while their pain levels and healing progress will be closely monitored through special X-ray scans before and after the procedures. It's important to note that certain individuals, such as smokers, pregnant or nursing mothers, and those with specific dental conditions, will not be eligible to participate. If you think you may qualify or are interested in helping researchers learn more about pain management in dental infections, this trial could be a good opportunity.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Patient must be ≥ 18-year-old
- • Patient must be systemically healthy; American Society of Anesthesiologists (ASA) Class I or II
- • Patient must exhibit clinical evidence of pulp necrosis and acute apical abscess
- • Patient must present with radiographic
- • signs of apical disease either by
- • periapical radiography or cone-beam
- • computed tomography
- • Patient consented to receive conventional pulpal debridement, incision and drainage at the end of the study
- • Persistent pain of moderate or higher level (\>4) was the main inclusion criterion. Pain assessed as follows: 0 defined as no pain, 1-3 as mild pain, 4-6 as moderate pain, and 7-10 as severe pain
- Exclusion Criteria:
- • Smokers (more than 10 cigarettes per day)
- • External or internal tooth resorption
- • Marginal periodontitis
- • Pregnant or nursing mothers (hormonal factors may influence the periapical condition)
- • Documented allergic or adverse reactions to amoxicillin or valacyclovir
- • Teeth with unusual anatomy or inaccurate clinical diagnosis on the day of treatment (i.e., partially necrotic pulp)
- • Patients currently taking antibiotics or antiviral medications
About University Of California, San Francisco
The University of California, San Francisco (UCSF) is a leading academic institution renowned for its commitment to advancing healthcare through innovative research and clinical trials. With a focus on translating scientific discoveries into effective therapies, UCSF collaborates with a diverse array of stakeholders, including healthcare professionals, industry partners, and patient communities. The university's research programs emphasize interdisciplinary approaches and leverage cutting-edge technology to address complex medical challenges. As a sponsor of clinical trials, UCSF is dedicated to maintaining the highest standards of ethical conduct and scientific rigor, ensuring the safety and well-being of participants while contributing to the broader medical knowledge base.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
San Francisco, California, United States
Patients applied
Trial Officials
Mike Sabeti, DDS
Principal Investigator
University of California, San Francisco
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Similar Trials