Herpes Simplex Treated With Antimicrobial Photodynamic Therapy: Randomized Controlled Trial
ABSTRACT Objective To compare the efficacy of antimicrobial photodynamic therapy (aPDT) with topical acyclovir in terms of healing time for herpes simplex lesions, recurrence rates, HSV‐1 quantification in secretion and saliva, pain levels, temperature changes, and outcomes measured by the Oral Heal...
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Published in | Journal of oral pathology & medicine Vol. 54; no. 7; pp. 547 - 555 |
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Main Authors | , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Denmark
Wiley Subscription Services, Inc
01.08.2025
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Subjects | |
Online Access | Get full text |
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Summary: | ABSTRACT
Objective
To compare the efficacy of antimicrobial photodynamic therapy (aPDT) with topical acyclovir in terms of healing time for herpes simplex lesions, recurrence rates, HSV‐1 quantification in secretion and saliva, pain levels, temperature changes, and outcomes measured by the Oral Health Impact Profile Questionnaire (OHIP‐14).
Subjects and Methods
Patients with vesicle or ulcer phase lesions were randomly divided into two groups: the control group (topical acyclovir four times daily for 7 days + aPDT simulation, n = 12) and the experimental group (placebo acyclovir ointment + aPDT applied once, n = 12). The primary outcome was lesion resolution time, with secondary assessments for recurrence, pain, local temperature, virus quantification via quantitative polymerase chain reaction (qPCR), and impact on quality of life.
Results
After 1 year, the remission and recurrence rates were similar between groups (p = 0.718 and p = 0.317, respectively), as were pain levels and temperature (p = 0.039 and 0.217). There was an increase in HSV‐1 viral load in saliva, measured by qPCR, on Day 3 in the ACV group (p = 0.043). The OHIP‐14 scores were similar between groups after 1 year.
Conclusion
This study found no differences between aPDT and topical acyclovir regarding lesion resolution time, recurrence rates, pain levels, local temperature changes, and OHIP‐14 scores. Both treatments showed similar efficacy in managing herpes simplex lesions over 1 year. While there was an increase in HSV‐1 viral load in saliva in the acyclovir group on Day 3, this did not translate into differences in clinical outcomes between the groups.
Trial Registration
NCT 04037475 |
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Bibliography: | Funding This work was supported by Conselho Nacional de Desenvolvimento Científico e Tecnológico (316287/2023‐7) and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (88887.624877/2021‐000). ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 0904-2512 1600-0714 1600-0714 |
DOI: | 10.1111/jop.13647 |